Aromatase Expression in Stromal Cells of Endometrioid Endometrial Cancer Correlates with Poor Survival

Purpose and Experimental Design: To assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55 patients with endometrial cancer were evaluated for expression of aromatase using immunohistochemistry, and the correlation between aromatase expressi...

Full description

Saved in:
Bibliographic Details
Published inClinical cancer research Vol. 11; no. 6; pp. 2188 - 2194
Main Authors SEGAWA, Tomoya, SHOZU, Makio, MURAKAMI, Kouich, KASAI, Tadayuki, SHINOHARA, Kazunori, NOMURA, Kazuhito, OHNO, Satoshi, INOUE, Masaki
Format Journal Article
LanguageEnglish
Published Philadelphia, PA American Association for Cancer Research 15.03.2005
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Purpose and Experimental Design: To assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55 patients with endometrial cancer were evaluated for expression of aromatase using immunohistochemistry, and the correlation between aromatase expression and clinicopathologic parameters were analyzed. Results: Immunohistochemical staining for aromatase was positive for 32 (58%), 20 (36%), and 19 (34%) patients in cancer epithelial cells, stromal cells, and myometrial cells around the flank invasion, respectively. In situ hybridization also detected aromatase mRNA in all three types of cells. RT-PCR analysis revealed that aromatase mRNA was 2.5 ± 1.0 amol/μg total RNA (mean ± SE; n = 7) in tumor tissue. Western blot analysis detected the expected aromatase protein size of 58 kDa in cancer tissues more abundantly than in cancer-free endometrium ( n = 3). The immunoreactivity in stromal cells correlated positively with advanced surgical stage and poor survival. Survival analysis revealed that the immunoreactivity of stromal cells was a significant prognostic factor, independent of histologic grade, muscular invasion, and lymph node metastasis, but dependent on surgical stage. By contrast, the immunoreactivity of aromatase both in cancer epithelial cells and myometrial cells did not correlate with prognosis. Conclusions: To the best of our knowledge, this is the first evidence associating intratumoral aromatase expression in stromal cells and poor survival in endometrioid endometrial cancer. This positive linkage indicates that local expression of aromatase plays a role in tumor progression through the formation of in situ estrogens. In situ expression of aromatase may offer a potential target for management of endometrial cancers.
AbstractList Abstract Purpose and Experimental Design: To assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55 patients with endometrial cancer were evaluated for expression of aromatase using immunohistochemistry, and the correlation between aromatase expression and clinicopathologic parameters were analyzed. Results: Immunohistochemical staining for aromatase was positive for 32 (58%), 20 (36%), and 19 (34%) patients in cancer epithelial cells, stromal cells, and myometrial cells around the flank invasion, respectively. In situ hybridization also detected aromatase mRNA in all three types of cells. RT-PCR analysis revealed that aromatase mRNA was 2.5 ± 1.0 amol/μg total RNA (mean ± SE; n = 7) in tumor tissue. Western blot analysis detected the expected aromatase protein size of 58 kDa in cancer tissues more abundantly than in cancer-free endometrium (n = 3). The immunoreactivity in stromal cells correlated positively with advanced surgical stage and poor survival. Survival analysis revealed that the immunoreactivity of stromal cells was a significant prognostic factor, independent of histologic grade, muscular invasion, and lymph node metastasis, but dependent on surgical stage. By contrast, the immunoreactivity of aromatase both in cancer epithelial cells and myometrial cells did not correlate with prognosis. Conclusions: To the best of our knowledge, this is the first evidence associating intratumoral aromatase expression in stromal cells and poor survival in endometrioid endometrial cancer. This positive linkage indicates that local expression of aromatase plays a role in tumor progression through the formation of in situ estrogens. In situ expression of aromatase may offer a potential target for management of endometrial cancers.
PURPOSE AND EXPERIMENTAL DESIGNTo assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55 patients with endometrial cancer were evaluated for expression of aromatase using immunohistochemistry, and the correlation between aromatase expression and clinicopathologic parameters were analyzed.RESULTSImmunohistochemical staining for aromatase was positive for 32 (58%), 20 (36%), and 19 (34%) patients in cancer epithelial cells, stromal cells, and myometrial cells around the flank invasion, respectively. In situ hybridization also detected aromatase mRNA in all three types of cells. RT-PCR analysis revealed that aromatase mRNA was 2.5 +/- 1.0 amol/mug total RNA (mean +/- SE; n = 7) in tumor tissue. Western blot analysis detected the expected aromatase protein size of 58 kDa in cancer tissues more abundantly than in cancer-free endometrium (n = 3). The immunoreactivity in stromal cells correlated positively with advanced surgical stage and poor survival. Survival analysis revealed that the immunoreactivity of stromal cells was a significant prognostic factor, independent of histologic grade, muscular invasion, and lymph node metastasis, but dependent on surgical stage. By contrast, the immunoreactivity of aromatase both in cancer epithelial cells and myometrial cells did not correlate with prognosis.CONCLUSIONSTo the best of our knowledge, this is the first evidence associating intratumoral aromatase expression in stromal cells and poor survival in endometrioid endometrial cancer. This positive linkage indicates that local expression of aromatase plays a role in tumor progression through the formation of in situ estrogens. In situ expression of aromatase may offer a potential target for management of endometrial cancers.
Purpose and Experimental Design: To assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55 patients with endometrial cancer were evaluated for expression of aromatase using immunohistochemistry, and the correlation between aromatase expression and clinicopathologic parameters were analyzed. Results: Immunohistochemical staining for aromatase was positive for 32 (58%), 20 (36%), and 19 (34%) patients in cancer epithelial cells, stromal cells, and myometrial cells around the flank invasion, respectively. In situ hybridization also detected aromatase mRNA in all three types of cells. RT-PCR analysis revealed that aromatase mRNA was 2.5 ± 1.0 amol/μg total RNA (mean ± SE; n = 7) in tumor tissue. Western blot analysis detected the expected aromatase protein size of 58 kDa in cancer tissues more abundantly than in cancer-free endometrium ( n = 3). The immunoreactivity in stromal cells correlated positively with advanced surgical stage and poor survival. Survival analysis revealed that the immunoreactivity of stromal cells was a significant prognostic factor, independent of histologic grade, muscular invasion, and lymph node metastasis, but dependent on surgical stage. By contrast, the immunoreactivity of aromatase both in cancer epithelial cells and myometrial cells did not correlate with prognosis. Conclusions: To the best of our knowledge, this is the first evidence associating intratumoral aromatase expression in stromal cells and poor survival in endometrioid endometrial cancer. This positive linkage indicates that local expression of aromatase plays a role in tumor progression through the formation of in situ estrogens. In situ expression of aromatase may offer a potential target for management of endometrial cancers.
To assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55 patients with endometrial cancer were evaluated for expression of aromatase using immunohistochemistry, and the correlation between aromatase expression and clinicopathologic parameters were analyzed. Immunohistochemical staining for aromatase was positive for 32 (58%), 20 (36%), and 19 (34%) patients in cancer epithelial cells, stromal cells, and myometrial cells around the flank invasion, respectively. In situ hybridization also detected aromatase mRNA in all three types of cells. RT-PCR analysis revealed that aromatase mRNA was 2.5 +/- 1.0 amol/mug total RNA (mean +/- SE; n = 7) in tumor tissue. Western blot analysis detected the expected aromatase protein size of 58 kDa in cancer tissues more abundantly than in cancer-free endometrium (n = 3). The immunoreactivity in stromal cells correlated positively with advanced surgical stage and poor survival. Survival analysis revealed that the immunoreactivity of stromal cells was a significant prognostic factor, independent of histologic grade, muscular invasion, and lymph node metastasis, but dependent on surgical stage. By contrast, the immunoreactivity of aromatase both in cancer epithelial cells and myometrial cells did not correlate with prognosis. To the best of our knowledge, this is the first evidence associating intratumoral aromatase expression in stromal cells and poor survival in endometrioid endometrial cancer. This positive linkage indicates that local expression of aromatase plays a role in tumor progression through the formation of in situ estrogens. In situ expression of aromatase may offer a potential target for management of endometrial cancers.
Author Tomoya Segawa
Tadayuki Kasai
Kazunori Shinohara
Makio Shozu
Kouich Murakami
Satoshi Ohno
Kazuhito Nomura
Masaki Inoue
Author_xml – sequence: 1
  givenname: Tomoya
  surname: SEGAWA
  fullname: SEGAWA, Tomoya
  organization: Department of Obstetrics and Gynecology, Kanazawa University School of Medicine, Kanazawa, Japan
– sequence: 2
  givenname: Makio
  surname: SHOZU
  fullname: SHOZU, Makio
  organization: Department of Obstetrics and Gynecology, Kanazawa University School of Medicine, Kanazawa, Japan
– sequence: 3
  givenname: Kouich
  surname: MURAKAMI
  fullname: MURAKAMI, Kouich
  organization: Department of Obstetrics and Gynecology, Kanazawa University School of Medicine, Kanazawa, Japan
– sequence: 4
  givenname: Tadayuki
  surname: KASAI
  fullname: KASAI, Tadayuki
  organization: Department of Obstetrics and Gynecology, Kanazawa University School of Medicine, Kanazawa, Japan
– sequence: 5
  givenname: Kazunori
  surname: SHINOHARA
  fullname: SHINOHARA, Kazunori
  organization: Department of Obstetrics and Gynecology, Kanazawa University School of Medicine, Kanazawa, Japan
– sequence: 6
  givenname: Kazuhito
  surname: NOMURA
  fullname: NOMURA, Kazuhito
  organization: Department of Obstetrics and Gynecology, Kanazawa University School of Medicine, Kanazawa, Japan
– sequence: 7
  givenname: Satoshi
  surname: OHNO
  fullname: OHNO, Satoshi
  organization: Department of Obstetrics and Gynecology, Kanazawa University School of Medicine, Kanazawa, Japan
– sequence: 8
  givenname: Masaki
  surname: INOUE
  fullname: INOUE, Masaki
  organization: Department of Obstetrics and Gynecology, Kanazawa University School of Medicine, Kanazawa, Japan
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16626003$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/15788666$$D View this record in MEDLINE/PubMed
BookMark eNpFkctuGyEYRlGVqInTPkIrNo2yGRfMdZbRyLlIkRol7Rox-KemmhlcGMfN24epHXnFhzgfl8MMnQxxAIS-UDKnVOjvlChdEc4W86Z5KqGiWtQf0DkVQlVsIcVJye_MGZrl_IcQyinhH9EZFUprKeU58tcp9na0GfDy3yZBziEOOAz4eZwWOtxA12UcPV4Oq9jDmEIMq-NkIuzgIOEmpgSdHSHjXRjX-DHGhJ-36SW82O4TOvW2y_D5MF6gXzfLn81d9fDj9r65fqgcU2Ssaqa1kNpyRbwlzjLNfc3bthZOgpI1aFYr5zStrVBcWL_yrarblquWc68cu0CX-303Kf7dQh5NH7IrT7ADxG02UgleiqSAYg-6FHNO4M0mhd6mV0OJmQSbSZ6Z5JkiuAQzCS69r4cDtm0Pq2PrYLQA3w6Azc52PhU7IR85KReSEFa4qz23Dr_Xu5DAuP8eyxeATW5dLmGkWVCt2RsGUpSg
CitedBy_id crossref_primary_10_1111_jog_13743
crossref_primary_10_1016_j_canlet_2008_10_008
crossref_primary_10_1111_j_1365_2559_2007_02612_x
crossref_primary_10_1002_ijc_28679
crossref_primary_10_1007_s10517_006_0397_4
crossref_primary_10_3390_cancers13092149
crossref_primary_10_1016_j_ygyno_2013_09_023
crossref_primary_10_1007_s11010_021_04099_0
crossref_primary_10_1517_13543784_2011_566862
crossref_primary_10_1002_path_5004
crossref_primary_10_1177_2470289718801379
crossref_primary_10_3390_ijms19103276
crossref_primary_10_1186_s13048_023_01201_6
crossref_primary_10_1093_molehr_gaad017
crossref_primary_10_1016_j_mce_2013_07_026
crossref_primary_10_2478_v10039_012_0055_1
crossref_primary_10_1016_j_mce_2018_10_004
crossref_primary_10_1016_j_mce_2010_11_023
crossref_primary_10_1111_j_1440_1789_2009_01047_x
crossref_primary_10_1186_1477_7827_7_102
crossref_primary_10_3389_fphar_2017_00368
crossref_primary_10_1507_endocrj_KR_114
crossref_primary_10_3390_biom12111624
crossref_primary_10_1007_s00129_006_1864_8
crossref_primary_10_1515_HMBCI_2010_027
crossref_primary_10_3390_ijms19020611
crossref_primary_10_1530_ERC_15_0470
crossref_primary_10_1016_j_ygyno_2018_10_024
crossref_primary_10_1016_j_mce_2005_10_013
crossref_primary_10_3389_fendo_2023_1156680
crossref_primary_10_1016_j_steroids_2007_09_003
crossref_primary_10_1002_med_20131
crossref_primary_10_1016_j_bbalip_2019_08_008
crossref_primary_10_1111_IGC_0b013e3181a47c25
crossref_primary_10_1007_s13277_013_0991_9
crossref_primary_10_1080_15384047_2017_1414762
crossref_primary_10_1158_0008_5472_CAN_09_4653
crossref_primary_10_1196_annals_1397_010
crossref_primary_10_3389_fphar_2018_00940
crossref_primary_10_1016_j_fertnstert_2005_12_057
Cites_doi 10.1006/gyno.2000.5865
10.1016/0022-4731(86)90362-6
10.1210/jcem.79.6.7989490
10.1177/1071557601008001S21
10.1210/jcem.87.8.8733
10.1023/A:1020531329686
10.1016/0960-0760(93)90251-Q
10.1016/S0378-5122(98)00034-6
10.1016/S0301-2115(02)00147-1
10.1517/13543784.12.3.337
10.1023/A:1006029612990
10.1210/jc.83.4.1319
10.1016/0022-4731(90)90167-Q
10.1111/j.1349-7006.1994.tb02365.x
10.1210/jc.86.7.3436
10.1007/s00432-003-0427-9
10.1677/erc.0.0060197
10.1023/A:1006009128920
10.1097/00042192-199805040-00004
10.1016/S0378-5122(02)00140-8
10.1023/A:1006033813899
10.1210/endo.141.10.7719
10.1210/jcem-62-3-508
10.1093/jnci/88.16.1127
10.1016/0378-5122(86)90008-3
10.1046/j.1471-0528.2003.02389.x
10.1016/S1359-6349(04)90893-2
10.1016/S0960-0760(03)00363-7
10.1210/jcem-55-5-1029
10.1016/0022-4731(89)90408-1
10.1016/0046-8177(94)90127-9
ContentType Journal Article
Copyright 2005 INIST-CNRS
Copyright_xml – notice: 2005 INIST-CNRS
DBID IQODW
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7X8
DOI 10.1158/1078-0432.CCR-04-1859
DatabaseName Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
MEDLINE - Academic
DatabaseTitleList CrossRef
MEDLINE - Academic

MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1557-3265
EndPage 2194
ExternalDocumentID 10_1158_1078_0432_CCR_04_1859
15788666
16626003
11_6_2188
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID -
08R
29B
2WC
34G
39C
3O-
53G
55
5GY
5RE
5VS
AAPBV
ABFLS
ABOCM
ACIWK
ACPRK
ADACO
ADBBV
ADBIT
AENEX
AETEA
AFFNX
AFRAH
ALMA_UNASSIGNED_HOLDINGS
BAWUL
C1A
CS3
DIK
DU5
E3Z
EBS
EJD
F5P
FH7
FRP
GJ
GX1
H13
H~9
IH2
KQ8
L7B
LSO
MVM
O0-
OHT
OK1
P0W
P2P
RCR
RHF
RHI
RNS
SJN
UDS
VH1
W2D
WOQ
X7M
XFK
XJT
ZA5
ZCG
ZGI
---
.55
.GJ
18M
1CY
2FS
476
4H-
6J9
ACGFO
ADCOW
ADGIM
ADNWM
AFHIN
AFOSN
AI.
BR6
BTFSW
IQODW
J5H
QTD
TR2
W8F
WHG
YKV
ACSVP
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7X8
ID FETCH-LOGICAL-c370t-9388568a470fa0ca384f94bb95c6e769e8397cc819a5745afdfb79bb47b44f7c3
ISSN 1078-0432
IngestDate Fri Aug 16 22:39:03 EDT 2024
Fri Aug 23 02:13:00 EDT 2024
Sun Jul 28 06:58:00 EDT 2024
Fri Nov 25 01:06:22 EST 2022
Fri Jan 15 20:33:59 EST 2021
IsPeerReviewed true
IsScholarly true
Issue 6
Keywords Endometrium cancer
Enzyme
Uterine diseases
Stromal cell
Estrogen synthase
Malignant tumor
Gene expression
Survival
Female genital diseases
Language English
License CC BY 4.0
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c370t-9388568a470fa0ca384f94bb95c6e769e8397cc819a5745afdfb79bb47b44f7c3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 15788666
PQID 67547450
PQPubID 23479
PageCount 7
ParticipantIDs proquest_miscellaneous_67547450
crossref_primary_10_1158_1078_0432_CCR_04_1859
pubmed_primary_15788666
pascalfrancis_primary_16626003
highwire_cancerresearch_11_6_2188
ProviderPackageCode RHF
RHI
PublicationCentury 2000
PublicationDate 2005-03-15
PublicationDateYYYYMMDD 2005-03-15
PublicationDate_xml – month: 03
  year: 2005
  text: 2005-03-15
  day: 15
PublicationDecade 2000
PublicationPlace Philadelphia, PA
PublicationPlace_xml – name: Philadelphia, PA
– name: United States
PublicationTitle Clinical cancer research
PublicationTitleAlternate Clin Cancer Res
PublicationYear 2005
Publisher American Association for Cancer Research
Publisher_xml – name: American Association for Cancer Research
References 2022061104233027300_B19
2022061104233027300_B18
2022061104233027300_B17
2022061104233027300_B16
2022061104233027300_B11
2022061104233027300_B33
2022061104233027300_B10
2022061104233027300_B32
2022061104233027300_B31
2022061104233027300_B30
2022061104233027300_B15
2022061104233027300_B14
2022061104233027300_B13
2022061104233027300_B35
2022061104233027300_B12
2022061104233027300_B34
2022061104233027300_B4
2022061104233027300_B3
2022061104233027300_B6
2022061104233027300_B5
2022061104233027300_B8
2022061104233027300_B7
2022061104233027300_B9
2022061104233027300_B29
2022061104233027300_B28
2022061104233027300_B27
2022061104233027300_B2
2022061104233027300_B1
2022061104233027300_B22
2022061104233027300_B21
2022061104233027300_B20
2022061104233027300_B26
2022061104233027300_B25
2022061104233027300_B24
2022061104233027300_B23
References_xml – ident: 2022061104233027300_B35
  doi: 10.1006/gyno.2000.5865
– ident: 2022061104233027300_B5
  doi: 10.1016/0022-4731(86)90362-6
– ident: 2022061104233027300_B9
  doi: 10.1210/jcem.79.6.7989490
– ident: 2022061104233027300_B25
  doi: 10.1177/1071557601008001S21
– ident: 2022061104233027300_B15
  doi: 10.1210/jcem.87.8.8733
– ident: 2022061104233027300_B17
  doi: 10.1023/A:1020531329686
– ident: 2022061104233027300_B8
  doi: 10.1016/0960-0760(93)90251-Q
– ident: 2022061104233027300_B24
  doi: 10.1016/S0378-5122(98)00034-6
– ident: 2022061104233027300_B19
– ident: 2022061104233027300_B31
  doi: 10.1016/S0301-2115(02)00147-1
– ident: 2022061104233027300_B16
  doi: 10.1517/13543784.12.3.337
– ident: 2022061104233027300_B12
  doi: 10.1023/A:1006029612990
– ident: 2022061104233027300_B4
– ident: 2022061104233027300_B2
– ident: 2022061104233027300_B22
  doi: 10.1210/jc.83.4.1319
– ident: 2022061104233027300_B33
  doi: 10.1016/0022-4731(90)90167-Q
– ident: 2022061104233027300_B1
  doi: 10.1111/j.1349-7006.1994.tb02365.x
– ident: 2022061104233027300_B23
  doi: 10.1210/jc.86.7.3436
– ident: 2022061104233027300_B7
  doi: 10.1007/s00432-003-0427-9
– ident: 2022061104233027300_B10
– ident: 2022061104233027300_B32
  doi: 10.1677/erc.0.0060197
– ident: 2022061104233027300_B11
  doi: 10.1023/A:1006009128920
– ident: 2022061104233027300_B29
  doi: 10.1097/00042192-199805040-00004
– ident: 2022061104233027300_B27
  doi: 10.1016/S0378-5122(02)00140-8
– ident: 2022061104233027300_B13
  doi: 10.1023/A:1006033813899
– ident: 2022061104233027300_B14
  doi: 10.1210/endo.141.10.7719
– ident: 2022061104233027300_B26
  doi: 10.1210/jcem-62-3-508
– ident: 2022061104233027300_B3
  doi: 10.1093/jnci/88.16.1127
– ident: 2022061104233027300_B28
  doi: 10.1016/0378-5122(86)90008-3
– ident: 2022061104233027300_B30
  doi: 10.1046/j.1471-0528.2003.02389.x
– ident: 2022061104233027300_B34
  doi: 10.1016/S1359-6349(04)90893-2
– ident: 2022061104233027300_B20
  doi: 10.1016/S0960-0760(03)00363-7
– ident: 2022061104233027300_B21
  doi: 10.1210/jcem-55-5-1029
– ident: 2022061104233027300_B6
  doi: 10.1016/0022-4731(89)90408-1
– ident: 2022061104233027300_B18
  doi: 10.1016/0046-8177(94)90127-9
SSID ssj0014104
Score 2.0677881
Snippet Purpose and Experimental Design: To assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55 patients...
To assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55 patients with endometrial cancer were...
Abstract Purpose and Experimental Design: To assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55...
PURPOSE AND EXPERIMENTAL DESIGNTo assess the prognostic significance of intratumoral aromatase in endometrioid endometrial cancer, sections from 55 patients...
SourceID proquest
crossref
pubmed
pascalfrancis
highwire
SourceType Aggregation Database
Index Database
Publisher
StartPage 2188
SubjectTerms Antineoplastic agents
Aromatase - genetics
Aromatase - metabolism
Biological and medical sciences
Carcinoma, Endometrioid - diagnosis
Carcinoma, Endometrioid - enzymology
Disease Progression
Endometrium - enzymology
Epithelial Cells - enzymology
Epithelial Cells - pathology
Estrogen formation
Female
Female genital diseases
Gynecology. Andrology. Obstetrics
Humans
hybridization
immunohistochemistry
in situ
In Situ Hybridization
Lymphatic Metastasis - pathology
Medical sciences
Middle Aged
Myometrium - enzymology
Myometrium - pathology
Neoplasm Invasiveness - pathology
Pharmacology. Drug treatments
Prognosis
prognostic indicators
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - genetics
RNA, Messenger - metabolism
Stromal Cells - enzymology
survival analysis
Survival Rate
Tumors
Title Aromatase Expression in Stromal Cells of Endometrioid Endometrial Cancer Correlates with Poor Survival
URI http://clincancerres.aacrjournals.org/content/11/6/2188.abstract
https://www.ncbi.nlm.nih.gov/pubmed/15788666
https://search.proquest.com/docview/67547450
Volume 11
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Zb9NAEF6FIiFeEDfhKIvEW5Rgx7tr-7EKRYUqCLWp1Ddrvd5trTbeKgeo_X38MGYPH4EgFV4sx_Ex9vd5dnY8B0LvlRqnuYkLC5VKYILC6DCNYc5DJAx3ShYitK0Tpl_ZwQn5ckpPe72fnail9SofiZuteSX_gypsA1xNluw_INucFDbAOuALS0AYlrfCeG-hweCEcchULHYBrTZw8Xhl_rgcTOSlK468XxV6bnpn6bJof5g9DOgL0AoLm9QifbLbN60XoFNAjXz3MtTFDOpESuEO9LWCGp_yTM_1NQcNdMZ_NAp_ClaqHhyf65t1o9_1uhTnA4CZX_B52foPCn69vigHh3zJyw2PBDUhWS4ns5MEANqpQzAbM-lv6agrmdO6gSnzS7yjU3pNTEH7jV0jiUZVhx1Kbupd1xzwzwGBJtY34S8wmkyOzLcgsFLS7v6A69XcsiQEFZYwtqU892_DZhPMCDMolhkB7qC74zilxgXw8fNh8y2LhLaJZSODzyMDyT5slct2inJCbBpLdQFrE7_Ll4C1cr1X_j45skbS7CF64Gc3eM9R9RHqyeoxujf18RtPkGoYi1vG4rLCnrHYMhZrhbuMxR3GYgcvbhmLDWOxYSyuGfsUnXzan00Ohr7Tx1BEcbAaplGSUJZwEgeKB4JHCVEpyfOUCiZjlkow42MhwHrlNCaUq0LlcZrnJM4JUbGInqGdSlfyBcIJZ5EKGRNJERKaqyTksggiGQW5AHM07qNR_UizK1fQJbMTYZpkBo7MwJEBHLCSGTj66F394DP3btWvVtYg30e7G4i0Z2bGYRBEffS2higD_W0-yvFK6vUygwk7gVsK-ui5Q6491pPg5S0EeIXuuzfR-AZfo53VYi3fgLW8ynctGX8BUjXAkg
link.rule.ids 315,786,790,27957,27958
linkProvider Flying Publisher
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=Aromatase+Expression+in+Stromal+Cells+of+Endometrioid+Endometrial+Cancer+Correlates+with+Poor+Survival&rft.jtitle=Clinical+cancer+research&rft.au=Tomoya+Segawa&rft.au=Makio+Shozu&rft.au=Kouich+Murakami&rft.au=Tadayuki+Kasai&rft.date=2005-03-15&rft.pub=American+Association+for+Cancer+Research&rft.issn=1078-0432&rft.eissn=1557-3265&rft.volume=11&rft.issue=6&rft.spage=2188&rft_id=info:doi/10.1158%2F1078-0432.CCR-04-1859&rft_id=info%3Apmid%2F15788666&rft.externalDBID=n%2Fa&rft.externalDocID=11_6_2188
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1078-0432&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1078-0432&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1078-0432&client=summon