Presence of a mouse mammary tumour virus-like in feline lymphomas: a preliminary study

The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus, can cause murine thymic lymphomas. Interestingly, a MMTV-like virus is suspected to be involved in human breast cancer and feline mammary carcinomas....

Full description

Saved in:
Bibliographic Details
Published inInfectious agents and cancer Vol. 17; no. 1; pp. 1 - 11
Main Authors Parisi, Francesca, Lessi, Francesca, Menicagli, Michele, Civita, Prospero, Liotti, Romano, Millanta, Francesca, Freer, Giulia, Pistello, Mauro, Mazzanti, Chiara Maria, Poli, Alessandro
Format Journal Article
LanguageEnglish
Published London BioMed Central Ltd 23.06.2022
BioMed Central
BMC
Subjects
Online AccessGet full text

Cover

Loading…
Abstract The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus, can cause murine thymic lymphomas. Interestingly, a MMTV-like virus is suspected to be involved in human breast cancer and feline mammary carcinomas. However, to date, no cases of MMTV-like sequence amplifications have been described in lymphoid neoplasms in veterinary literature. The aim of this study was to investigate the presence of env nucleotide sequences and protein 14 (p14) of a MMTV-like virus in fifty-three feline lymphoma samples. Our results show that MMTV-like sequences were detected in 5/53 tumours (9.4%): three gastrointestinal lymphomas (one B-type diffuse large, one B-type small non-cleaved, and one T-type diffuse mixed lymphoma); and two nasal lymphomas (one B-type diffuse small cleaved lymphoma and one B-type diffuse mixed lymphoma). P14 expression was detected in the cytoplasm, and rarely in nuclei, exclusively of neoplastic cells from PCR-positive tumours. The correlation between the presence of the MMTV- env like sequences (MMTVels) and p14 antigen was statistically significant in nasal lymphomas. All cats with MMTVels-positive lymphoma had a history of contact with the outdoor environment and/or catteries, and two deceased subjects shared their environment with cats that also died of lymphoma. In conclusion, this study succeeds in demonstrating the presence of MMTVels and p14 in feline lymphomas. The characterization of the immunophenotype of MMTVels-positive lymphomas could contribute to the understanding of a possible role of a MMTV-like virus in feline tumour aetiology. The significant association between the presence of the viral sequences in lymphoid tumours and their nasal localization, together with the data collected through supplementary anamnesis, should be further analysed in order to understand the epidemiology of the virus.
AbstractList The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus, can cause murine thymic lymphomas. Interestingly, a MMTV-like virus is suspected to be involved in human breast cancer and feline mammary carcinomas. However, to date, no cases of MMTV-like sequence amplifications have been described in lymphoid neoplasms in veterinary literature. The aim of this study was to investigate the presence of env nucleotide sequences and protein 14 (p14) of a MMTV-like virus in fifty-three feline lymphoma samples. Our results show that MMTV-like sequences were detected in 5/53 tumours (9.4%): three gastrointestinal lymphomas (one B-type diffuse large, one B-type small non-cleaved, and one T-type diffuse mixed lymphoma); and two nasal lymphomas (one B-type diffuse small cleaved lymphoma and one B-type diffuse mixed lymphoma). P14 expression was detected in the cytoplasm, and rarely in nuclei, exclusively of neoplastic cells from PCR-positive tumours. The correlation between the presence of the MMTV-env like sequences (MMTVels) and p14 antigen was statistically significant in nasal lymphomas. All cats with MMTVels-positive lymphoma had a history of contact with the outdoor environment and/or catteries, and two deceased subjects shared their environment with cats that also died of lymphoma. In conclusion, this study succeeds in demonstrating the presence of MMTVels and p14 in feline lymphomas. The characterization of the immunophenotype of MMTVels-positive lymphomas could contribute to the understanding of a possible role of a MMTV-like virus in feline tumour aetiology. The significant association between the presence of the viral sequences in lymphoid tumours and their nasal localization, together with the data collected through supplementary anamnesis, should be further analysed in order to understand the epidemiology of the virus.The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus, can cause murine thymic lymphomas. Interestingly, a MMTV-like virus is suspected to be involved in human breast cancer and feline mammary carcinomas. However, to date, no cases of MMTV-like sequence amplifications have been described in lymphoid neoplasms in veterinary literature. The aim of this study was to investigate the presence of env nucleotide sequences and protein 14 (p14) of a MMTV-like virus in fifty-three feline lymphoma samples. Our results show that MMTV-like sequences were detected in 5/53 tumours (9.4%): three gastrointestinal lymphomas (one B-type diffuse large, one B-type small non-cleaved, and one T-type diffuse mixed lymphoma); and two nasal lymphomas (one B-type diffuse small cleaved lymphoma and one B-type diffuse mixed lymphoma). P14 expression was detected in the cytoplasm, and rarely in nuclei, exclusively of neoplastic cells from PCR-positive tumours. The correlation between the presence of the MMTV-env like sequences (MMTVels) and p14 antigen was statistically significant in nasal lymphomas. All cats with MMTVels-positive lymphoma had a history of contact with the outdoor environment and/or catteries, and two deceased subjects shared their environment with cats that also died of lymphoma. In conclusion, this study succeeds in demonstrating the presence of MMTVels and p14 in feline lymphomas. The characterization of the immunophenotype of MMTVels-positive lymphomas could contribute to the understanding of a possible role of a MMTV-like virus in feline tumour aetiology. The significant association between the presence of the viral sequences in lymphoid tumours and their nasal localization, together with the data collected through supplementary anamnesis, should be further analysed in order to understand the epidemiology of the virus.
The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus, can cause murine thymic lymphomas. Interestingly, a MMTV-like virus is suspected to be involved in human breast cancer and feline mammary carcinomas. However, to date, no cases of MMTV-like sequence amplifications have been described in lymphoid neoplasms in veterinary literature. The aim of this study was to investigate the presence of env nucleotide sequences and protein 14 (p14) of a MMTV-like virus in fifty-three feline lymphoma samples. Our results show that MMTV-like sequences were detected in 5/53 tumours (9.4%): three gastrointestinal lymphomas (one B-type diffuse large, one B-type small non-cleaved, and one T-type diffuse mixed lymphoma); and two nasal lymphomas (one B-type diffuse small cleaved lymphoma and one B-type diffuse mixed lymphoma). P14 expression was detected in the cytoplasm, and rarely in nuclei, exclusively of neoplastic cells from PCR-positive tumours. The correlation between the presence of the MMTV-env like sequences (MMTVels) and p14 antigen was statistically significant in nasal lymphomas. All cats with MMTVels-positive lymphoma had a history of contact with the outdoor environment and/or catteries, and two deceased subjects shared their environment with cats that also died of lymphoma. In conclusion, this study succeeds in demonstrating the presence of MMTVels and p14 in feline lymphomas. The characterization of the immunophenotype of MMTVels-positive lymphomas could contribute to the understanding of a possible role of a MMTV-like virus in feline tumour aetiology. The significant association between the presence of the viral sequences in lymphoid tumours and their nasal localization, together with the data collected through supplementary anamnesis, should be further analysed in order to understand the epidemiology of the virus.
Abstract The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus, can cause murine thymic lymphomas. Interestingly, a MMTV-like virus is suspected to be involved in human breast cancer and feline mammary carcinomas. However, to date, no cases of MMTV-like sequence amplifications have been described in lymphoid neoplasms in veterinary literature. The aim of this study was to investigate the presence of env nucleotide sequences and protein 14 (p14) of a MMTV-like virus in fifty-three feline lymphoma samples. Our results show that MMTV-like sequences were detected in 5/53 tumours (9.4%): three gastrointestinal lymphomas (one B-type diffuse large, one B-type small non-cleaved, and one T-type diffuse mixed lymphoma); and two nasal lymphomas (one B-type diffuse small cleaved lymphoma and one B-type diffuse mixed lymphoma). P14 expression was detected in the cytoplasm, and rarely in nuclei, exclusively of neoplastic cells from PCR-positive tumours. The correlation between the presence of the MMTV-env like sequences (MMTVels) and p14 antigen was statistically significant in nasal lymphomas. All cats with MMTVels-positive lymphoma had a history of contact with the outdoor environment and/or catteries, and two deceased subjects shared their environment with cats that also died of lymphoma. In conclusion, this study succeeds in demonstrating the presence of MMTVels and p14 in feline lymphomas. The characterization of the immunophenotype of MMTVels-positive lymphomas could contribute to the understanding of a possible role of a MMTV-like virus in feline tumour aetiology. The significant association between the presence of the viral sequences in lymphoid tumours and their nasal localization, together with the data collected through supplementary anamnesis, should be further analysed in order to understand the epidemiology of the virus.
The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus, can cause murine thymic lymphomas. Interestingly, a MMTV-like virus is suspected to be involved in human breast cancer and feline mammary carcinomas. However, to date, no cases of MMTV-like sequence amplifications have been described in lymphoid neoplasms in veterinary literature. The aim of this study was to investigate the presence of env nucleotide sequences and protein 14 (p14) of a MMTV-like virus in fifty-three feline lymphoma samples. Our results show that MMTV-like sequences were detected in 5/53 tumours (9.4%): three gastrointestinal lymphomas (one B-type diffuse large, one B-type small non-cleaved, and one T-type diffuse mixed lymphoma); and two nasal lymphomas (one B-type diffuse small cleaved lymphoma and one B-type diffuse mixed lymphoma). P14 expression was detected in the cytoplasm, and rarely in nuclei, exclusively of neoplastic cells from PCR-positive tumours. The correlation between the presence of the MMTV- env like sequences (MMTVels) and p14 antigen was statistically significant in nasal lymphomas. All cats with MMTVels-positive lymphoma had a history of contact with the outdoor environment and/or catteries, and two deceased subjects shared their environment with cats that also died of lymphoma. In conclusion, this study succeeds in demonstrating the presence of MMTVels and p14 in feline lymphomas. The characterization of the immunophenotype of MMTVels-positive lymphomas could contribute to the understanding of a possible role of a MMTV-like virus in feline tumour aetiology. The significant association between the presence of the viral sequences in lymphoid tumours and their nasal localization, together with the data collected through supplementary anamnesis, should be further analysed in order to understand the epidemiology of the virus.
The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus, can cause murine thymic lymphomas. Interestingly, a MMTV-like virus is suspected to be involved in human breast cancer and feline mammary carcinomas. However, to date, no cases of MMTV-like sequence amplifications have been described in lymphoid neoplasms in veterinary literature. The aim of this study was to investigate the presence of env nucleotide sequences and protein 14 (p14) of a MMTV-like virus in fifty-three feline lymphoma samples. Our results show that MMTV-like sequences were detected in 5/53 tumours (9.4%): three gastrointestinal lymphomas (one B-type diffuse large, one B-type small non-cleaved, and one T-type diffuse mixed lymphoma); and two nasal lymphomas (one B-type diffuse small cleaved lymphoma and one B-type diffuse mixed lymphoma). P14 expression was detected in the cytoplasm, and rarely in nuclei, exclusively of neoplastic cells from PCR-positive tumours. The correlation between the presence of the MMTV-env like sequences (MMTVels) and p14 antigen was statistically significant in nasal lymphomas. All cats with MMTVels-positive lymphoma had a history of contact with the outdoor environment and/or catteries, and two deceased subjects shared their environment with cats that also died of lymphoma. In conclusion, this study succeeds in demonstrating the presence of MMTVels and p14 in feline lymphomas. The characterization of the immunophenotype of MMTVels-positive lymphomas could contribute to the understanding of a possible role of a MMTV-like virus in feline tumour aetiology. The significant association between the presence of the viral sequences in lymphoid tumours and their nasal localization, together with the data collected through supplementary anamnesis, should be further analysed in order to understand the epidemiology of the virus. Keywords: MMTV-like virus, Feline lymphoma, Immunohistochemistry, Fragment analysis, Heminested PCR
ArticleNumber 35
Audience Academic
Author Liotti, Romano
Lessi, Francesca
Mazzanti, Chiara Maria
Freer, Giulia
Pistello, Mauro
Millanta, Francesca
Parisi, Francesca
Civita, Prospero
Menicagli, Michele
Poli, Alessandro
Author_xml – sequence: 1
  givenname: Francesca
  surname: Parisi
  fullname: Parisi, Francesca
– sequence: 2
  givenname: Francesca
  surname: Lessi
  fullname: Lessi, Francesca
– sequence: 3
  givenname: Michele
  surname: Menicagli
  fullname: Menicagli, Michele
– sequence: 4
  givenname: Prospero
  surname: Civita
  fullname: Civita, Prospero
– sequence: 5
  givenname: Romano
  surname: Liotti
  fullname: Liotti, Romano
– sequence: 6
  givenname: Francesca
  surname: Millanta
  fullname: Millanta, Francesca
– sequence: 7
  givenname: Giulia
  surname: Freer
  fullname: Freer, Giulia
– sequence: 8
  givenname: Mauro
  surname: Pistello
  fullname: Pistello, Mauro
– sequence: 9
  givenname: Chiara Maria
  surname: Mazzanti
  fullname: Mazzanti, Chiara Maria
– sequence: 10
  givenname: Alessandro
  orcidid: 0000-0003-1254-5772
  surname: Poli
  fullname: Poli, Alessandro
BookMark eNp9Uk1v1DAUjFAR_YA_wCkSFy4p_kpsc0CqKqCVKsEBuFpe-2XrJbEXO6m0_56XbkXZCiEfbD_PjN8bzWl1FFOEqnpNyTmlqntXKCdMNoSxhhAhdKOfVSdUtqTRXKqjv87H1WkpGwQpptSL6pi3kuuOsJPqx9cMBaKDOvW1rcc0F6hHO4427-ppxnuu70KeSzOEn1CHWPcwhAj1sBu3t2m05T3SthmLY4gLqUyz372snvd2KPDqYT-rvn_6-O3yqrn58vn68uKmcaJtdcOd7Bih1FICvLW-5bxdMQqd6JR3gumVbmXPrAavPfOW05VmtOMULLUeBD-rrve6PtmN2eaw9G2SDea-kPLa2DwFN4DphUK3eumZ04LbdkUck7JVTisvwCvU-rDX2s6rEbyDOGU7HIgevsRwa9bpzmBLmjKKAm8fBHL6NUOZzBiKg2GwEdBXwzpFCdeESIS-eQLdoNMRrUIUinVUcvGIWlscIMQ-4b9uETUXkigqmBIL6vwfKFwexuAwMn3A-gGB7Qkup1Iy9H9mpMQsyTL7ZBlMlrlPltFIUk9ILkx2CmnxIgz_o_4G6rnRVg
CitedBy_id crossref_primary_10_3390_v14112435
crossref_primary_10_3390_vetsci9090467
crossref_primary_10_1186_s13027_023_00518_7
Cites_doi 10.3892/ijmm.8.5.573
10.1128/JVI.32.1.251-258.1979
10.1002/jemt.20233
10.1016/0167-5699(94)90317-4
10.1128/JVI.62.12.4644-4652.1988
10.1093/jnci/36.4.685
10.1158/1541-7786.MCR-11-0581
10.3389/fonc.2018.00141
10.3390/ani11102821
10.1002/ijc.2910250515
10.1016/0022-2836(73)90070-3
10.1128/JCM.01157-10
10.1186/1742-4690-7-108
10.1002/path.1997
10.3390/v2092000
10.1016/j.ajpath.2011.06.046
10.1016/0042-6822(87)90128-0
10.1158/1078-0432.CCR-03-0364
10.1385/MO:20:3:233
10.1128/JVI.42.3.804-813.1982
10.1371/journal.pone.0176280
10.1128/JVI.49.1.92-101.1984
10.1158/0008-5472.CAN-04-3879
10.1128/JVI.64.6.2474-2483.1990
10.1016/s1286-4579(00)01275-2
10.1016/0304-3835(94)03671-5
10.1016/0042-6822(80)90333-5
10.1128/mcb.5.4.823-830.1985
10.3390/v14050977
10.1146/annurev.iy.13.040195.002331
10.1002/cncr.20436
10.1128/JVI.64.9.4043-4050.1990
10.18632/oncotarget.7762
10.1186/s13027-021-00383-2
10.18632/oncotarget.4567
10.1016/0277-5379(83)90071-8
10.1016/0042-6822(87)90345-x
10.1093/aje/153.11.1079
10.1371/journal.pone.0200839
10.1016/s0306-9877(02)00204-9
10.1016/s0039-6109(05)70066-9
10.1128/JVI.43.3.819-829.1982
10.1084/jem.185.10.1871
10.1177/0300985811404712
10.1002/1097-0142(19820515)49:10<2112::AID-CNCR2820491024>3.0.CO;2-2
10.1016/j.micpath.2019.03.021
10.1128/jvi.77.6.3866-3870.2003
ContentType Journal Article
Copyright COPYRIGHT 2022 BioMed Central Ltd.
2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2022. The Author(s).
The Author(s) 2022
Copyright_xml – notice: COPYRIGHT 2022 BioMed Central Ltd.
– notice: 2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2022. The Author(s).
– notice: The Author(s) 2022
DBID AAYXX
CITATION
3V.
7TO
7U9
7X7
7XB
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FYUFA
GHDGH
H94
K9.
M0S
PHGZM
PHGZT
PIMPY
PKEHL
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
DOA
DOI 10.1186/s13027-022-00449-9
DatabaseName CrossRef
ProQuest Central (Corporate)
Oncogenes and Growth Factors Abstracts
Virology and AIDS Abstracts
ProQuest Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Health & Medical Collection (Alumni Edition)
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
Publicly Available Content Database
Virology and AIDS Abstracts
Oncogenes and Growth Factors Abstracts
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest One Academic Eastern Edition
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Central China
ProQuest Hospital Collection (Alumni)
ProQuest Central
ProQuest Health & Medical Complete
Health Research Premium Collection
ProQuest One Academic UKI Edition
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
AIDS and Cancer Research Abstracts
ProQuest Central (New)
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic


CrossRef


Publicly Available Content Database
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1750-9378
EndPage 11
ExternalDocumentID oai_doaj_org_article_f48027f7d2c943a5b0c27758c98d4ed8
PMC9219121
A708142844
10_1186_s13027_022_00449_9
GeographicLocations United States--US
Italy
GeographicLocations_xml – name: United States--US
– name: Italy
GroupedDBID ---
0R~
29I
2WC
53G
5GY
5VS
7X7
8FI
8FJ
AAFWJ
AAJSJ
AASML
AAWTL
AAYXX
ABDBF
ABUWG
ACGFO
ACPRK
ACUHS
ADBBV
ADRAZ
ADUKV
AENEX
AFKRA
AFPKN
AHBYD
AHMBA
AHYZX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BCNDV
BENPR
BFQNJ
BMC
BPHCQ
BVXVI
C6C
CCPQU
CITATION
CS3
DIK
DU5
E3Z
EBD
EBLON
EBS
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
IAO
IHR
INH
INR
ITC
KQ8
M48
M~E
O5R
O5S
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
RBZ
RNS
ROL
RPM
RSV
SBL
SOJ
TR2
TUS
UKHRP
WOQ
WOW
~8M
PMFND
3V.
7TO
7U9
7XB
8FK
AZQEC
DWQXO
H94
K9.
PKEHL
PQEST
PQUKI
PRINS
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c4559-3c762011a10e35ad5335b21e6468dc429b957f2a9ed9d2da31b921631ea1ade43
IEDL.DBID M48
ISSN 1750-9378
IngestDate Wed Aug 27 01:27:19 EDT 2025
Thu Aug 21 18:45:57 EDT 2025
Thu Jul 10 23:47:33 EDT 2025
Sun Jun 29 13:12:42 EDT 2025
Tue Jun 17 21:33:38 EDT 2025
Tue Jun 10 20:47:29 EDT 2025
Tue Jul 01 02:03:59 EDT 2025
Thu Apr 24 22:53:30 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
License Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c4559-3c762011a10e35ad5335b21e6468dc429b957f2a9ed9d2da31b921631ea1ade43
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
content type line 23
ORCID 0000-0003-1254-5772
OpenAccessLink https://www.proquest.com/docview/2691261734?pq-origsite=%requestingapplication%
PMID 35739602
PQID 2691261734
PQPubID 54871
PageCount 11
ParticipantIDs doaj_primary_oai_doaj_org_article_f48027f7d2c943a5b0c27758c98d4ed8
pubmedcentral_primary_oai_pubmedcentral_nih_gov_9219121
proquest_miscellaneous_2681039007
proquest_journals_2691261734
gale_infotracmisc_A708142844
gale_infotracacademiconefile_A708142844
crossref_primary_10_1186_s13027_022_00449_9
crossref_citationtrail_10_1186_s13027_022_00449_9
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20220623
PublicationDateYYYYMMDD 2022-06-23
PublicationDate_xml – month: 6
  year: 2022
  text: 20220623
  day: 23
PublicationDecade 2020
PublicationPlace London
PublicationPlace_xml – name: London
PublicationTitle Infectious agents and cancer
PublicationYear 2022
Publisher BioMed Central Ltd
BioMed Central
BMC
Publisher_xml – name: BioMed Central Ltd
– name: BioMed Central
– name: BMC
References WTL Lee (449_CR48) 1987; 159
AB Valldya (449_CR16) 1980; 104
S Yanagawa (449_CR50) 1990; 64
MJ Robinson (449_CR26) 2010; 7
F Mustafa (449_CR4) 2003; 77
F Zammarchi (449_CR32) 2006; 209
J Wolfhart (449_CR43) 2001; 153
K Bielawski (449_CR30) 2001; 8
ML Gemignani (449_CR42) 1999; 79
MC Mazzanti (449_CR29) 2015; 21
R Michalides (449_CR17) 1982; 43
R Nusse (449_CR15) 1979; 32
O Braitbard (449_CR38) 2016; 7
H Acha-Orbea (449_CR1) 1995; 13
449_CR27
P Civita (449_CR23) 2018; 13
PH Levine (449_CR40) 2004; 15
FL Wang (449_CR44) 2021; 16
D Velin (449_CR53) 1997; 185
WL Hsu (449_CR22) 2010; 48
PR Etkind (449_CR52) 2004; 10
JK Ball (449_CR3) 1987; 161
S Szabo (449_CR21) 2005; 68
B Felluga (449_CR5) 1969; 43
J Racevskis (449_CR34) 1990; 64
R Michalides (449_CR47) 1985; 5
S Imai (449_CR13) 1983; 19
SR Ross (449_CR2) 2000; 2
CE Ford (449_CR39) 2002; 9
AB Vaidya (449_CR45) 1980; 104
F Parisi (449_CR9) 2022; 14
O Muhlbock (449_CR10) 1950; 10
F Parisi (449_CR24) 2021; 11
W Held (449_CR6) 1994; 15
MK Amarante (449_CR36) 2019; 130
CL Hsu (449_CR49) 1988; 62
J Racevskis (449_CR33) 1982; 42
P Etkind (449_CR51) 2000; 6
D Feldman (449_CR37) 2012; 10
J Dudley (449_CR46) 1984; 49
Y Wang (449_CR41) 2003; 20
SR Ross (449_CR8) 2012; 2
N Einaga (449_CR31) 2017; 12
A Matsuzawa (449_CR7) 1995; 90
JS Lawson (449_CR19) 2018; 8
PF Moore (449_CR28) 2012; 49
HE Varmus (449_CR14) 1973; 1973
DK Howard (449_CR25) 1980; 25
M Cotterchio (449_CR20) 2002; 59
MC Mazzanti (449_CR18) 2011; 179
GH Smith (449_CR11) 1965; 36
A Bar-Sinai (449_CR35) 2005; 65
Y Tsubura (449_CR12) 1981; 72
References_xml – volume: 43
  start-page: 319
  year: 1969
  ident: 449_CR5
  publication-title: J Natl Cancer Inst
– volume: 8
  start-page: 573
  issue: 5
  year: 2001
  ident: 449_CR30
  publication-title: Int J Mol Med
  doi: 10.3892/ijmm.8.5.573
– volume: 32
  start-page: 251
  issue: 1
  year: 1979
  ident: 449_CR15
  publication-title: J Virol
  doi: 10.1128/JVI.32.1.251-258.1979
– volume: 68
  start-page: 209
  issue: 3–4
  year: 2005
  ident: 449_CR21
  publication-title: Microsc Res Tech
  doi: 10.1002/jemt.20233
– volume: 15
  start-page: 184
  year: 1994
  ident: 449_CR6
  publication-title: Immunol Today
  doi: 10.1016/0167-5699(94)90317-4
– volume: 62
  start-page: 4644
  issue: 12
  year: 1988
  ident: 449_CR49
  publication-title: J Virol
  doi: 10.1128/JVI.62.12.4644-4652.1988
– volume: 36
  start-page: 685
  year: 1965
  ident: 449_CR11
  publication-title: J Natl Cancer Inst
  doi: 10.1093/jnci/36.4.685
– volume: 10
  start-page: 1077
  issue: 8
  year: 2012
  ident: 449_CR37
  publication-title: Mol Cancer Res
  doi: 10.1158/1541-7786.MCR-11-0581
– volume: 8
  start-page: 141
  year: 2018
  ident: 449_CR19
  publication-title: Front Oncol
  doi: 10.3389/fonc.2018.00141
– volume: 11
  start-page: 2821
  issue: 10
  year: 2021
  ident: 449_CR24
  publication-title: Animals
  doi: 10.3390/ani11102821
– volume: 25
  start-page: 647
  year: 1980
  ident: 449_CR25
  publication-title: Int J Cancer
  doi: 10.1002/ijc.2910250515
– volume: 1973
  start-page: 663
  issue: 79
  year: 1973
  ident: 449_CR14
  publication-title: J Mol Biol
  doi: 10.1016/0022-2836(73)90070-3
– volume: 48
  start-page: 4354
  issue: 12
  year: 2010
  ident: 449_CR22
  publication-title: J Clin Microbiol
  doi: 10.1128/JCM.01157-10
– volume: 7
  start-page: 108
  year: 2010
  ident: 449_CR26
  publication-title: Retrovirology
  doi: 10.1186/1742-4690-7-108
– volume: 209
  start-page: 436
  year: 2006
  ident: 449_CR32
  publication-title: J Pathol
  doi: 10.1002/path.1997
– volume: 2
  start-page: 2000
  issue: 9
  year: 2012
  ident: 449_CR8
  publication-title: Viruses
  doi: 10.3390/v2092000
– volume: 179
  start-page: 2083
  year: 2011
  ident: 449_CR18
  publication-title: Am J Pathol
  doi: 10.1016/j.ajpath.2011.06.046
– volume: 161
  start-page: 357
  year: 1987
  ident: 449_CR3
  publication-title: Virology
  doi: 10.1016/0042-6822(87)90128-0
– volume: 10
  start-page: 5656
  year: 2004
  ident: 449_CR52
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.CCR-03-0364
– volume: 20
  start-page: 233
  year: 2003
  ident: 449_CR41
  publication-title: Med Oncol
  doi: 10.1385/MO:20:3:233
– volume: 42
  start-page: 804
  issue: 3
  year: 1982
  ident: 449_CR33
  publication-title: J Virol
  doi: 10.1128/JVI.42.3.804-813.1982
– volume: 12
  start-page: e0176280
  issue: 5
  year: 2017
  ident: 449_CR31
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0176280
– volume: 49
  start-page: 92
  issue: 1
  year: 1984
  ident: 449_CR46
  publication-title: J Virol
  doi: 10.1128/JVI.49.1.92-101.1984
– volume: 65
  start-page: 7223
  issue: 16
  year: 2005
  ident: 449_CR35
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-04-3879
– volume: 64
  start-page: 2474
  issue: 6
  year: 1990
  ident: 449_CR50
  publication-title: J Virol
  doi: 10.1128/JVI.64.6.2474-2483.1990
– volume: 2
  start-page: 1215
  year: 2000
  ident: 449_CR2
  publication-title: Microbes Infect
  doi: 10.1016/s1286-4579(00)01275-2
– volume: 90
  start-page: 3
  issue: 1
  year: 1995
  ident: 449_CR7
  publication-title: Cancer Lett
  doi: 10.1016/0304-3835(94)03671-5
– volume: 104
  start-page: 279
  year: 1980
  ident: 449_CR45
  publication-title: Virology
  doi: 10.1016/0042-6822(80)90333-5
– volume: 5
  start-page: 823
  issue: 4
  year: 1985
  ident: 449_CR47
  publication-title: Mol Cell Biol
  doi: 10.1128/mcb.5.4.823-830.1985
– volume: 14
  start-page: 977
  year: 2022
  ident: 449_CR9
  publication-title: Viruses
  doi: 10.3390/v14050977
– volume: 13
  start-page: 459
  year: 1995
  ident: 449_CR1
  publication-title: Annu Rev Immunol
  doi: 10.1146/annurev.iy.13.040195.002331
– volume: 15
  start-page: 721
  issue: 101
  year: 2004
  ident: 449_CR40
  publication-title: Cancer
  doi: 10.1002/cncr.20436
– volume: 64
  start-page: 4043
  year: 1990
  ident: 449_CR34
  publication-title: J Virol
  doi: 10.1128/JVI.64.9.4043-4050.1990
– volume: 7
  start-page: 21168
  issue: 16
  year: 2016
  ident: 449_CR38
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.7762
– volume: 16
  start-page: 47
  year: 2021
  ident: 449_CR44
  publication-title: Infect Agent Cancer
  doi: 10.1186/s13027-021-00383-2
– volume: 21
  start-page: 18355
  year: 2015
  ident: 449_CR29
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.4567
– volume: 104
  start-page: 279
  year: 1980
  ident: 449_CR16
  publication-title: Virology
  doi: 10.1016/0042-6822(80)90333-5
– volume: 19
  start-page: 1011
  year: 1983
  ident: 449_CR13
  publication-title: Eur J Cancer Clin Oncol
  doi: 10.1016/0277-5379(83)90071-8
– volume: 159
  start-page: 39
  issue: 1
  year: 1987
  ident: 449_CR48
  publication-title: Virology
  doi: 10.1016/0042-6822(87)90345-x
– volume: 153
  start-page: 1079
  year: 2001
  ident: 449_CR43
  publication-title: Am J Epidemiol
  doi: 10.1093/aje/153.11.1079
– volume: 13
  start-page: 1
  issue: 7
  year: 2018
  ident: 449_CR23
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0200839
– volume: 9
  start-page: 1118
  year: 2002
  ident: 449_CR39
  publication-title: Clin Cancer Res
– volume: 59
  start-page: 492
  issue: 4
  year: 2002
  ident: 449_CR20
  publication-title: Med Hypotheses
  doi: 10.1016/s0306-9877(02)00204-9
– volume: 79
  start-page: 1157
  year: 1999
  ident: 449_CR42
  publication-title: Surg Clin North America
  doi: 10.1016/s0039-6109(05)70066-9
– volume: 10
  start-page: 861
  year: 1950
  ident: 449_CR10
  publication-title: J Natl Cancer Inst
– volume: 43
  start-page: 819
  issue: 3
  year: 1982
  ident: 449_CR17
  publication-title: J Virol
  doi: 10.1128/JVI.43.3.819-829.1982
– volume: 6
  start-page: 1273
  year: 2000
  ident: 449_CR51
  publication-title: Clin Cancer Res
– volume: 185
  start-page: 1871
  issue: 10
  year: 1997
  ident: 449_CR53
  publication-title: J Exp Med
  doi: 10.1084/jem.185.10.1871
– volume: 49
  start-page: 658
  issue: 4
  year: 2012
  ident: 449_CR28
  publication-title: Vet Pathol
  doi: 10.1177/0300985811404712
– volume: 72
  start-page: 424
  year: 1981
  ident: 449_CR12
  publication-title: Gan
– ident: 449_CR27
  doi: 10.1002/1097-0142(19820515)49:10<2112::AID-CNCR2820491024>3.0.CO;2-2
– volume: 130
  start-page: 283
  year: 2019
  ident: 449_CR36
  publication-title: Microb Pathog
  doi: 10.1016/j.micpath.2019.03.021
– volume: 77
  start-page: 3866
  year: 2003
  ident: 449_CR4
  publication-title: J Virol
  doi: 10.1128/jvi.77.6.3866-3870.2003
SSID ssj0048288
Score 2.2646341
SecondaryResourceType review_article
Snippet The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus, can cause...
Abstract The mouse mammary tumour virus (MMTV) is implicated in the aetiology of murine mammary carcinomas and a variant of it, the type B leukemogenic virus,...
SourceID doaj
pubmedcentral
proquest
gale
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Enrichment Source
Index Database
StartPage 1
SubjectTerms Analysis
Antibodies
Antigens
B cells
Breast cancer
Cytoplasm
Dendritic cells
Epidemiology
Etiology
Feline lymphoma
Fragment analysis
Genetic testing
Heminested PCR
Immunohistochemistry
Infections
Localization
Lymphocytes
Lymphoma
Lymphomas
Mammary gland
Mitochondrial DNA
MMTV-like virus
Neoplasia
Peptides
Proteins
Review
Statistical analysis
Thymus
Tumor viruses
Tumors
Viruses
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NaxUxEA-lB-lFrFZcbSWC0IOE7ibZZOOtFUsRKh6s9BbyMcGHr9vyPoT-906y-x5dBb143E2ym8xHMsPM_ELIWy91F4NLTHa1Z-hvRGaCaFkSEe3rZFruc0T38rO6uJKfrtvrB1d95ZywAR54INxJwo9wnXTkwUjhWl8HrtHIDaaLEmIp88Uzb-NMDXuwRD-i25TIdOpkWcJzLGeu5wimYWZyDBW0_j_35N_zJB8cPOdPyOPRYqSnw0z3yQ70T8mjyzEm_ox8-1IqiALQ20Qdza480BtXatLoao3PC_pztlgv2Xz2A-ispynXoAOd3yMnc3rQexx2t8CXN6U4lxbI2QNydf7x64cLNt6WwIJEt4CJgPsaaqtrahCti2jHtZ43oKRCbuCx402rE3cGook8OtF4w9Eaa8A1LoIUz8luf9vDC0I9T7qOXKgQaulF6jSA4rr2AlTtoa5IsyGeDSOUeL7RYm6LS9EpOxDcIsFtIbg1FXm3HXM3AGn8tfdZ5sm2ZwbBLi9QNOwoGvZfolGR48xRm1UVpxfcWHGAi8ygV_ZUoz2E7peUFTmc9EQVC9PmjUzYUcWXlivTZDh7gc1vts15ZE5b6wG5jX26HGpHO6wieiJLk5VNW_rZ9wLzjdzBPzQv_wcpXpE9XqRfMS4Oye5qsYYjtKZW_nVRnF9tZxsG
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: ProQuest Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1LixQxEA66gngRn9juKhEEDxK2O0l3Ol5kFZdFWPHgytxCnjo42zPOQ9h_b1UmM9oKe-w8SCdVlVSlqr4Q8tJJ1QdvE5N97RjYG4FpL1qWRAD9OumWO_Tonn_qzi7kx0k7KRduqxJWudsT80Yd5h7vyI95pxtEDxfy7eInw1ej0LtantC4SW4hdBmGdKnJ3uCSYE30u0SZvjteZScdw_h19GNqpkeHUcbs_39n_jda8q_j5_QeuVv0RnqyJfR9ciMOD8jt8-IZf0i-fs55RD7SeaKWokEf6aXNmWl0vYHvJf01XW5WbDb9Eel0oAkz0SOdXQE9MUjoDXRbLKHwMqfo0gw8-4hcnH748v6MlTcTmJdgHDDhYXcDmbVNHUVrA2hzreNN7GQHNIHDx-lWJW51DDrwYEXjNAedrIm2sSFK8ZgcDPMhPiHU8aTqwEXnfS2dSL2KseOqdiJ2tYt1RZrd4hlfAMXxXYuZyYZF35ntghtYcJMX3OiKvN73WWzhNK5t_Q5psm-JUNi5YL78ZopkmQRcxlVSgXsthW1d7bkCK8jrPsgY-oq8QooaFFj4PW9L3gFMEqGvzIkCrQiMMCkrcjRqCYLmx9U7njBF0FfmD1tW5MW-Gnti8NoQgdrQpkeHO2hjFVEjXhrNbFwzTL9nsG-gDozQPL1-8ENyh2e-7hgXR-RgvdzEZ6Atrd3zLBK_Aez9Eqc
  priority: 102
  providerName: ProQuest
Title Presence of a mouse mammary tumour virus-like in feline lymphomas: a preliminary study
URI https://www.proquest.com/docview/2691261734
https://www.proquest.com/docview/2681039007
https://pubmed.ncbi.nlm.nih.gov/PMC9219121
https://doaj.org/article/f48027f7d2c943a5b0c27758c98d4ed8
Volume 17
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfR1ra9swUPQBY1_GnsxrFzQY7MPQZkuyZQ3GSEdLCaSUbRn5JvRyF5Y6rZOM9d_vpNhh3ko_GVuSLd1Dd-d7CKHXhovSWV0RXqaGgL3hiLQsJxVzoF9XMqcmeHTHZ8XphI-m-XQHdccdtQBc3mrahfOkJs383e_rm0_A8B8jw5fF-2V0vpEQlx78k5LIXbQPkkkERh3zrVeBg3URU-NAShIQy2WXRHPrO3qCKtbz_3_X_jeS8i_RdPIQPWh1SjzcEMEjtOPrx-jeuPWaP0Hfz2OOkfV4UWGNg7Hv8aWOWWt4tYb7Bv-aNeslmc9-ejyrcRWy1D2e3wCuQwDRBxh21cDDy5i-i2NR2qdocnL87fMpac9TIJaD4UCYhZ0P-FlnqWe5dqDp5YZmvuAF4AsEk5G5qKiW3klHnWaZkRT0tczrTDvP2TO0Vy9q_xxhQyuROsoKa1NuWFUK7wsqUsN8kRqfJijrgKdsW2w8nHkxV9HoKAu1AbgCgKsIcCUT9HY75mpTauPO3kcBJ9ueoUx2fLBoLlTLdaoCCqSiEo5ayZnOTWqpAAvJytJx78oEvQkYVYG8YHpWtzkJsMhQFksNBWhMYKBxnqDDXk9gQttv7mhCdTSsaCGzUPCeQfOrbXMYGQLbag_Yhj5lcMaDppYg0aOl3sr6LfXsRywEDtiBL2Qv7p7bAbpPI10XhLJDtLdq1v4laFIrM0C7YioGaH84HH0dwfXo-Oz8yyD-lxhE1vkD-I4caw
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtR3ZbtQwcFS2EvCCOEWggJFAPCCrie0cRkKohVYt7a4q1KK-ufERWLHNLnuA-lN8I2NvshCQ-tbHxHbizOWZzAXwQou8sKasqChiTdHesFQantKKW9SvK5ky7T26_UG2dyI-nqana_CrzYXxYZWtTAyC2o6N_0e-yTKZ-OrhXLybfKe-a5T3rrYtNJZkceAufqLJNnu7_wHx-5Kx3Z3j93u06SpAjUD1mXKD_I9UXSax42lpUd9JNUtcJjLcNYpnLdO8YqV0VlpmS55oyVBrSVyZlNYJjs-9BuuCoynTg_XtncHRp1b2C7RfijY1p8g2Z8EtSH3EvPecSio7x1_oEvD_WfBvfOZfB97ubbjVaKpka0lad2DN1Xfher_xxd-Dz0chc8k4Mq5ISfwvBEfOy5ALR-YLvJ6SH8PpYkZHw2-ODGtS-dx3R0YXSEE-LOkNLptM8eZ5SAomodTtfTi5Eng-gF49rt1DIJpVeWwZz4yJheZVkTuXsTzW3GWxdnEESQs8ZZoS5r6TxkgFU6bI1BLgCgGuAsCVjOD1as1kWcDj0tnbHiermb74drgxnn5RDS-rCuma5VVumZGCl6mODcvR7jKysMLZIoJXHqPKiwjcnimbTAf8SF9sS23lqIeh2SdEBBudmcjapjvc0oRqRMtM_WGECJ6vhv1KHy5XO8Q2zim8ix_1vwjyDi11vqw7Ug-_hvLiiB18Q_Lo8pc_gxt7x_1Ddbg_OHgMN1mg8YwyvgG9-XThnqCuNtdPGwYhcHbVPPkbS6ZPpA
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Presence+of+a+mouse+mammary+tumour+virus-like+in+feline+lymphomas%3A+a+preliminary+study&rft.jtitle=Infectious+agents+and+cancer&rft.au=Parisi%2C+Francesca&rft.au=Lessi%2C+Francesca&rft.au=Menicagli%2C+Michele&rft.au=Civita%2C+Prospero&rft.date=2022-06-23&rft.pub=BioMed+Central+Ltd&rft.issn=1750-9378&rft.eissn=1750-9378&rft.volume=17&rft.issue=1&rft_id=info:doi/10.1186%2Fs13027-022-00449-9&rft.externalDocID=A708142844
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1750-9378&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1750-9378&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1750-9378&client=summon