Distinct patterns of deletion on 10p and 10q suggest involvement of multiple tumor suppressor genes in the development of astrocytic gliomas of different malignancy grades

Deletions of chromosome 10 are the most frequent genetic abnormality in glioblastomas. Several commonly deleted regions have been proposed; however, they are not coincident. We have deletion mapped chromosome 10 in 198 astrocytic gliomas using 53 microsatellite markers. Two commonly deleted regions...

Full description

Saved in:
Bibliographic Details
Published inGenes chromosomes & cancer Vol. 22; no. 1; pp. 9 - 15
Main Authors Ichimura, Koichi, Schmidt, Esther E., Miyakawa, Ayako, Goike, Helena M., Collins, V. Peter
Format Journal Article
LanguageEnglish
Published New York Wiley Subscription Services, Inc., A Wiley Company 01.05.1998
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Deletions of chromosome 10 are the most frequent genetic abnormality in glioblastomas. Several commonly deleted regions have been proposed; however, they are not coincident. We have deletion mapped chromosome 10 in 198 astrocytic gliomas using 53 microsatellite markers. Two commonly deleted regions on 10p were identified, one of which lies between D10S594 and D10S559 and the other between D10S1713 and D10S189. Most of 10q deletions were large and included a region distal to D10S554. Four glioblastomas of 122 had patterns suggestive of homozygous deletions at D10S541, a locus close and distally located to the PTEN/MMAC1 gene. Losses of alleles were found not only in glioblastomas (93%) but also in anaplastic astrocytomas (66%) and in astrocytomas (35%). Most glioblastomas lost one entire chromosome 10, while astrocytomas preferentially lost only 10p. The data suggest that a number of tumor suppressor genes on chromosome 10, in addition to PTEN/MMAC1, may be associated with astrocytic glioma development. Genes Chromosomes Cancer 22:9–15, 1998. © 1998 Wiley‐Liss, Inc.
AbstractList Deletions of chromosome 10 are the most frequent genetic abnormality in glioblastomas. Several commonly deleted regions have been proposed; however, they are not coincident. We have deletion mapped chromosome 10 in 198 astrocytic gliomas using 53 microsatellite markers. Two commonly deleted regions on 10p were identified, one of which lies between D10S594 and D10S559 and the other between D10S1713 and D10S189. Most of 10q deletions were large and included a region distal to D10S554. Four glioblastomas of 122 had patterns suggestive of homozygous deletions at D10S541, a locus close and distally located to the PTEN/MMAC1 gene. Losses of alleles were found not only in glioblastomas (93%) but also in anaplastic astrocytomas (66%) and in astrocytomas (35%). Most glioblastomas lost one entire chromosome 10, while astrocytomas preferentially lost only 10p. The data suggest that a number of tumor suppressor genes on chromosome 10, in addition to PTEN/MMAC1, may be associated with astrocytic glioma development. Genes Chromosomes Cancer 22:9–15, 1998. © 1998 Wiley‐Liss, Inc.
Deletions of chromosome 10 are the most frequent genetic abnormality in glioblastomas. Several commonly deleted regions have been proposed; however, they are not coincident. We have deletion mapped chromosome 10 in 198 astrocytic gliomas using 53 microsatellite markers. Two commonly deleted regions on 10p were identified, one of which lies between D10S594 and D10S559 and the other between D10S1713 and D10S189. Most of 10q deletions were large and included a region distal to D10S554. Four glioblastomas of 122 had patterns suggestive of homozygous deletions at D10S541, a locus close and distally located to the PTEN/MMAC1 gene. Losses of alleles were found not only in glioblastomas (93%) but also in anaplastic astrocytomas (66%) and in astrocytomas (35%). Most glioblastomas lost one entire chromosome 10, while astrocytomas preferentially lost only 10p. The data suggest that a number of tumor suppressor genes on chromosome 10, in addition to PTEN/MMAC1, may be associated with astrocytic glioma development.
Author Goike, Helena M.
Collins, V. Peter
Ichimura, Koichi
Schmidt, Esther E.
Miyakawa, Ayako
Author_xml – sequence: 1
  givenname: Koichi
  surname: Ichimura
  fullname: Ichimura, Koichi
  organization: Ludwig Institute for Cancer Research and Unit of Tumor Pathology, Department of Oncology and Pathology, Karolinska Hospital, 171 76 Stockholm, Sweden
– sequence: 2
  givenname: Esther E.
  surname: Schmidt
  fullname: Schmidt, Esther E.
  organization: Ludwig Institute for Cancer Research and Unit of Tumor Pathology, Department of Oncology and Pathology, Karolinska Hospital, 171 76 Stockholm, Sweden
– sequence: 3
  givenname: Ayako
  surname: Miyakawa
  fullname: Miyakawa, Ayako
  organization: Ludwig Institute for Cancer Research and Unit of Tumor Pathology, Department of Oncology and Pathology, Karolinska Hospital, 171 76 Stockholm, Sweden
– sequence: 4
  givenname: Helena M.
  surname: Goike
  fullname: Goike, Helena M.
  organization: Ludwig Institute for Cancer Research and Unit of Tumor Pathology, Department of Oncology and Pathology, Karolinska Hospital, 171 76 Stockholm, Sweden
– sequence: 5
  givenname: V. Peter
  surname: Collins
  fullname: Collins, V. Peter
  email: vpc@instpat.ks.se
  organization: Ludwig Institute for Cancer Research and Unit of Tumor Pathology, Department of Oncology and Pathology, Karolinska Hospital, 171 76 Stockholm, Sweden
BackLink https://www.ncbi.nlm.nih.gov/pubmed/9591629$$D View this record in MEDLINE/PubMed
BookMark eNp9kl9v0zAUxSM0NLbBR0DKE9oeUmznj-OCkKYUSqeJSgXE45Wb3ARD4mS2M-hn4kvi0FIeQEiW7rF1fI6sn8-DE91rDII5JTNKCHt--X5VrK4oEXnEWJZcUiFykl4xNqcvxXx-vVpEy6Jgr-IZmRXrFyyiD4Kzo_1k0knqdcofBefWfiGEZLFIT4NTkQqaMXEW_Fgo65QuXThI59BoG_Z1WGGLTvU69IuSIZS68vMutGPToHWh0vd9e48dajfZu7F1amgxdGPXG-8aBoPWetmgRuvtofuMPvUe2374fUtaZ_py51QZNq3qO7mvVnWNZrJ0slWNlrrchY2RFdrHwcNathafHOZF8PHN6w_F2-h2vVwV17dRmcYJi5KslCiEIDkvk7iqtpwnQjKsCc1qXuV5lohtLjCrKi5FlpM8ZQnnmNFSCpls44vg2T53MP3d6N8LnbIltq3U2I8WuMhzllPujZu9sTS9tQZrGIzqpNkBJTARBJgIwoQEJiSwJ-g1UBAAniBMBCEGAsUa_LEPfXpoH7cdVsfIA7I_pd9Ui7u_Gv9b-I--X3sfGu1D_W_A78dQab5CxmOewqd3S7hhNxu62FBI4p9kI8lB
Cites_doi 10.1006/geno.1996.0277
10.1002/gcc.2870070311
10.1002/gcc.2870050111
10.1126/science.275.5308.1943
10.1016/0360-3016(93)90203-8
10.1038/ng1095-210
10.1007/BF00219686
10.1111/j.1349-7006.1996.tb00231.x
10.1016/0888-7543(89)90302-9
10.1038/ng0497-356
10.1126/science.270.5244.1945
10.3171/jns.1992.77.2.0295
10.1002/gcc.2870120404
10.1038/bjc.1997.2
10.1038/380152a0
10.1002/gcc.2870050412
ContentType Journal Article
Copyright Copyright © 1998 Wiley‐Liss, Inc.
Copyright_xml – notice: Copyright © 1998 Wiley‐Liss, Inc.
DBID BSCLL
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7X8
DOI 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1
DatabaseName Istex
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
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
Biology
EISSN 1098-2264
EndPage 15
ExternalDocumentID 10_1002__SICI_1098_2264_199805_22_1_9__AID_GCC2_3_0_CO_2_1
9591629
GCC2
ark_67375_WNG_J2JR1DR1_4
Genre article
Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: Swedish Cancer Society
– fundername: Axel and Margaret Axson Johnsons Funds
– fundername: Stockholm's Cancer Society
– fundername: Funds of the Karolinska Institute
– fundername: King Gustav V. Jubilee Fund
GroupedDBID ---
.3N
.GA
.GJ
.Y3
05W
0R~
10A
1L6
1OB
1OC
1ZS
31~
33P
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5GY
5VS
66C
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A01
A03
AAESR
AAEVG
AAHHS
AAJUZ
AANLZ
AAONW
AASGY
AAVGM
AAXRX
AAZKR
ABCQN
ABCUV
ABCVL
ABEFU
ABEML
ABHUG
ABIJN
ABJNI
ABLJU
ABPVW
ABQWH
ABWRO
ABXGK
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACFBH
ACGFS
ACGOF
ACMXC
ACPOU
ACPRK
ACSCC
ACXBN
ACXME
ACXQS
ADAWD
ADBBV
ADBTR
ADDAD
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFNX
AFFPM
AFGKR
AFPWT
AFRAH
AFVGU
AFZJQ
AGJLS
AHBTC
AHMBA
AIACR
AIURR
AIWBW
AJBDE
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ASPBG
ATUGU
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BSCLL
BY8
C45
CS3
D-6
D-7
D-E
D-F
DCZOG
DPXWK
DR2
DRFUL
DRMAN
DRSTM
DU5
EBD
EBS
EJD
EMOBN
F00
F01
F04
F5P
FEDTE
FUBAC
G-S
G.N
GLUZI
GNP
GODZA
H.X
HBH
HF~
HHY
HHZ
HVGLF
HZ~
IX1
J0M
JPC
KBYEO
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
M6P
MEWTI
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OVD
P2P
P2W
P2X
P2Z
P4B
P4D
PALCI
PQQKQ
Q.N
Q11
QB0
QRW
R.K
RIWAO
RJQFR
ROL
RWI
RX1
RYL
SAMSI
SUPJJ
SV3
TEORI
UB1
V2E
V8K
W8V
W99
WBKPD
WHWMO
WIB
WIH
WIJ
WIK
WJL
WOHZO
WQJ
WRC
WUP
WVDHM
WWO
WXI
WXSBR
XG1
XPP
XV2
ZGI
ZZTAW
~IA
~WT
AITYG
HGLYW
OIG
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7X8
ID FETCH-LOGICAL-c5342-46cae999087c43ddb7749a2ef016f7d88649b89e6dd7a9680852477e61ca9a4b3
IEDL.DBID DR2
ISSN 1045-2257
IngestDate Fri Aug 16 21:23:52 EDT 2024
Fri Aug 23 03:04:27 EDT 2024
Sat Sep 28 07:40:26 EDT 2024
Sat Aug 24 00:55:49 EDT 2024
Wed Jan 17 05:00:47 EST 2024
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c5342-46cae999087c43ddb7749a2ef016f7d88649b89e6dd7a9680852477e61ca9a4b3
Notes ArticleID:GCC2
Stockholm's Cancer Society
Axel and Margaret Axson Johnsons Funds
ark:/67375/WNG-J2JR1DR1-4
Swedish Cancer Society
istex:7CFDD3FEFA5559C96808ED16AA34F3FD6DC7D79B
Funds of the Karolinska Institute
King Gustav V. Jubilee Fund
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/%28SICI%291098-2264%28199805%2922%3A1%3C9%3A%3AAID-GCC2%3E3.0.CO%3B2-1
PMID 9591629
PQID 79882817
PQPubID 23479
PageCount 7
ParticipantIDs proquest_miscellaneous_79882817
crossref_primary_10_1002__SICI_1098_2264_199805_22_1_9__AID_GCC2_3_0_CO_2_1
pubmed_primary_9591629
wiley_primary_10_1002_SICI_1098_2264_199805_22_1_9_AID_GCC2_3_0_CO_2_1_GCC2
istex_primary_ark_67375_WNG_J2JR1DR1_4
PublicationCentury 1900
PublicationDate 1998-05
May 1998
1998-May
1998-05-00
19980501
PublicationDateYYYYMMDD 1998-05-01
PublicationDate_xml – month: 05
  year: 1998
  text: 1998-05
PublicationDecade 1990
PublicationPlace New York
PublicationPlace_xml – name: New York
– name: United States
PublicationTitle Genes chromosomes & cancer
PublicationTitleAlternate Genes Chromosom. Cancer
PublicationYear 1998
Publisher Wiley Subscription Services, Inc., A Wiley Company
Publisher_xml – name: Wiley Subscription Services, Inc., A Wiley Company
References Fujimoto M, Fults DW, Thomas GA, Nakamura Y, Heilbrun MP, White R, Story JL, Naylor SL, Kagan-Hallet KS, Sheridan PJ (1989) Loss of heterozygosity on chromosome 10 in human glioblastoma multiforme. Genomics 4: 210-214.
Hudson TJ, Stein LD, Gerety SS, Ma J, Castle AB, Silva J, Slonim DK, Baptista R, Kruglyak L, Xu SH, Hu X, Colbert A, Rosenberg C, Reeve-Daly MP, Rozen S, Hui L, Wu X, Vestergaard C, Wilson K, Bae J, Maitra S, Ganiatsas S, Evans C, DeAngelis M, Ingalls K, Nahf R, Horton L, Oskin M, Collymore A, Ye W, Kouyoumjian V, Zernsteva I, Tarn J, Devine R, Courtney D, Renaud M, Nguyen H, O'Connor T, Fizames C, Faure S, Gyapay G, Dib C, Morissette J, Orlin J, Birren B, Goodman N, Weissenbach J, Hawkins T, Foote S, Page D, Lander E (1995) An STS-based map of the human genome, with supplementary data from the Whitehead Institute/MIT Center for Genome Research, Human Genetic Mapping Project, Data Release 11 (October 1996). Science 270: 1945-1954.
Tokiyoshi K, Yoshimine T, Maruno M, Muhammad A, Hayakawa T (1996) Accumulation of allelic losses on chromosome 10 in human gliomas at recurrence. J Clin Pathol: Mol Pathol 49: M218-M222.
Ichimura K, Schmidt EE, Goike HM, Collins VP (1996) Human glioblastomas with no alterations of the CDKN2A (p16INK4A, MTS1) and CDK4 genes have frequent mutations of the retinoblastoma gene. Oncogene 13: 1065-1072.
Pershouse MA, Stubblefield E, Hadi A, Killary AM, Yung WK, Steck PA (1993) Analysis of the functional role of chromosome 10 loss in human glioblastomas. Cancer Res 53: 5043-5050.
Steck PA, Ligon AH, Cheong P, Yung WK, Pershouse MA (1995) Two tumor suppressive loci on chromosome 10 involved in human glioblastomas. Genes Chromosomes Cancer 12: 255-261.
Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette J, Weissenbach J (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380: 152-154.
von Deimling A, Louis DN, von Ammon K, Petersen I, Hoell T, Chung RY, Martuza RL, Schoenfeld DA, Yasargil MG, Wiestler OD, et al. (1992) Association of epidermal growth factor receptor gene amplification with loss of chromosome 10 in human glioblastoma multiforme. J Neurosurg 77: 295-301.
Cairns P, Polascik TJ, Eby Y, Tokino K, Califano J, Merlo A, Mao L, Herath J, Jenkins R, Westra W, Rutter JL, Buckler A, Gabrielson E, Tockman M, Cho KR, Hedrick L, Bova GS, Isaacs W, Koch W, Schwab D, Sidransky D (1995) Frequency of homozygous deletion at p16/CDKN2 in primary human tumours. Nat Genet 11: 210-212.
Kimmelman AC, Ross DA, Liang BC (1996) Loss of heterozygosity of chromosome 10p in human gliomas. Genomics 34: 250-254.
Rasheed BKA, Fuller GN, Friedman AH, Bigner DD, Bigner SH (1992) Loss of heterozygosity for 10q loci in human gliomas. Genes Chromosomes Cancer 5: 75-82.
Albarosa R, Colombo BM, Roz L, Magnani I, Pollo B, Cirenei N, Giani C, Conti AM, DiDonato S, Finocchiaro G (1996) Deletion mapping of gliomas suggests the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q. Am J Hum Genet 58: 1260-1267.
Simpson JR, Horton J, Scott C, Curran WJ, Rubin P, Fischbach J, Isaacson S, Rotman M, Asbell SO, Nelson JS, et al. (1993) Influence of location and extent of surgical resection on survival of patients with glioblastoma multiforme: Results of three consecutive Radiation Therapy Oncology Group (RTOG) clinical trials. Int J Rad Oncol Biol Phys 26: 239-244.
Fults D, Pedone C (1993) Deletion mapping of the long arm of chromosome 10 in glioblastoma multiforme. Genes Chromosomes Cancer 7: 173-177.
Karlbom AE, James CD, Boethius J, Cavenee WK, Collins VP, Nordenskjold M, Larsson C (1993) Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10. Hum Genet 92: 169-174.
Sonoda Y, Murakami Y, Tominaga T, Kayama T, Yoshimoto T, Sekiya T (1996) Deletion mapping of chromosome 10 in human glioma. Jpn J Cancer Res 87: 363-367.
Schmidt EE, Ichimura K, Messerle KR, Goike HM, Collins VP (1997) Infrequent methylation of CDKN2A(MTS1/p16) and rare mutation of both CDKN2A and CDKN2B(MTS2/p15) in primary astrocytic tumours. Br J Cancer 75: 2-8.
Steck PA, Pershouse MA, Jasser SA, Yung WKA, Lin H, Ligon AH, Langford LA, Baumgard ML, Hattier T, Davis T, Frye C, Hu R, Swedlund B, Teng DHF, Tavtigian SV (1997) Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat Genet 15: 356-362.
Ransom DT, Ritland SR, Moertel CA, Dahl RJ, O'Fallon JR, Scheithauer BW, Kimmel DW, Kelly PJ, Olopade OI, Diaz MO, et al. (1992) Correlation of cytogenetic analysis and loss of heterozygosity studies in human diffuse astrocytomas and mixed oligo-astrocytomas. Genes Chromosomes Cancer 5: 357-374.
Rasheed BKA, McLendon RE, Friedman HS, Friedman AH, Fuchs HE, Bigner DD, Bigner SH (1995) Chromosome 10 deletion mapping in human gliomas: A common deletion region in 10q25. Oncogene 10: 2243-2246.
Fults D, Pedone CA, Thomas GA, White R (1990) Allelotype of human malignant astrocytoma. Cancer Res 50: 5784-5789.
Russell DS, Rubinstein LJ (1989) Tumours of central neuroepithelial origin Pathology of Tumours of the Nervous System, 5th Ed. London: Edward Arnold, pp. 83-350.
James CD, Carlbom E, Dumanski JP, Hansen M, Nordenskjold M, Collins VP, Cavenee WK (1988) Clonal genomic alterations in glioma malignancy stages. Cancer Res 48: 5546-5551.
Li J, Yen C, Liaw D, Podsypanina K, Bose S, Wang SI, Puc J, Miliaresis C, Rodgers L, McCombie R, Bigner SH, Giovanella BC, Ittmann M, Tycko B, Hibshoosh H, Wigler MH, Parsons R (1997) PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science 275: 1943-1947.
1993; 7
1993; 26
1989; 4
1997; 75
1993; 92
1997; 15
1988; 48
1997; 275
1995; 12
1995; 11
1993; 53
1995; 10
1996; 380
1993
1996; 58
1996; 13
1996; 49
1992; 77
1996; 87
1995; 270
1996; 34
1989
1990; 50
1992; 5
Ransom (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB15) 1992; 5
Fults (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB5) 1993; 7
Ichimura (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB8) 1996; 13
Rasheed (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB16) 1992; 5
Li (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB13) 1997; 275
Fults (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB6) 1990; 50
Tokiyoshi (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB24) 1996; 49
Steck (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB23) 1997; 15
Russell (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB18) 1989
Simpson (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB20) 1993; 26
Schmidt (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB19) 1997; 75
Kimmelman (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB11) 1996; 34
Steck (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB22) 1995; 12
von Deimling (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB25) 1992; 77
Albarosa (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB1) 1996; 58
Dib (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB3) 1996; 380
James (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB9) 1988; 48
Kleihues (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB12) 1993
Cairns (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB2) 1995; 11
Sonoda (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB21) 1996; 87
Pershouse (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB14) 1993; 53
Karlbom (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB10) 1993; 92
Rasheed (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB17) 1995; 10
Hudson (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB7) 1995; 270
Fujimoto (10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB4) 1989; 4
References_xml – start-page: 83
  year: 1989
  end-page: 350
– volume: 13
  start-page: 1065
  year: 1996
  end-page: 1072
  article-title: Human glioblastomas with no alterations of the ) and genes have frequent mutations of the retinoblastoma gene
  publication-title: Oncogene
– volume: 380
  start-page: 152
  year: 1996
  end-page: 154
  article-title: A comprehensive genetic map of the human genome based on 5,264 microsatellites
  publication-title: Nature
– volume: 92
  start-page: 169
  year: 1993
  end-page: 174
  article-title: Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10
  publication-title: Hum Genet
– volume: 4
  start-page: 210
  year: 1989
  end-page: 214
  article-title: Loss of heterozygosity on chromosome 10 in human glioblastoma multiforme
  publication-title: Genomics
– volume: 50
  start-page: 5784
  year: 1990
  end-page: 5789
  article-title: Allelotype of human malignant astrocytoma
  publication-title: Cancer Res
– volume: 26
  start-page: 239
  year: 1993
  end-page: 244
  article-title: Influence of location and extent of surgical resection on survival of patients with glioblastoma multiforme: Results of three consecutive Radiation Therapy Oncology Group (RTOG) clinical trials
  publication-title: Int J Rad Oncol Biol Phys
– volume: 270
  start-page: 1945
  year: 1995
  end-page: 1954
  article-title: An STS‐based map of the human genome, with supplementary data from the Whitehead Institute/MIT Center for Genome Research, Human Genetic Mapping Project, Data Release 11 (October 1996)
  publication-title: Science
– volume: 5
  start-page: 357
  year: 1992
  end-page: 374
  article-title: Correlation of cytogenetic analysis and loss of heterozygosity studies in human diffuse astrocytomas and mixed oligo‐astrocytomas
  publication-title: Genes Chromosomes Cancer
– volume: 10
  start-page: 2243
  year: 1995
  end-page: 2246
  article-title: Chromosome 10 deletion mapping in human gliomas: A common deletion region in 10q25
  publication-title: Oncogene
– volume: 53
  start-page: 5043
  year: 1993
  end-page: 5050
  article-title: Analysis of the functional role of chromosome 10 loss in human glioblastomas
  publication-title: Cancer Res
– volume: 11
  start-page: 210
  year: 1995
  end-page: 212
  article-title: Frequency of homozygous deletion at in primary human tumours
  publication-title: Nat Genet
– volume: 34
  start-page: 250
  year: 1996
  end-page: 254
  article-title: Loss of heterozygosity of chromosome 10p in human gliomas
  publication-title: Genomics
– volume: 77
  start-page: 295
  year: 1992
  end-page: 301
  article-title: Association of epidermal growth factor receptor gene amplification with loss of chromosome 10 in human glioblastoma multiforme
  publication-title: J Neurosurg
– volume: 5
  start-page: 75
  year: 1992
  end-page: 82
  article-title: Loss of heterozygosity for 10q loci in human gliomas
  publication-title: Genes Chromosomes Cancer
– volume: 275
  start-page: 1943
  year: 1997
  end-page: 1947
  article-title: , a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
  publication-title: Science
– volume: 75
  start-page: 2
  year: 1997
  end-page: 8
  article-title: Infrequent methylation of ) and rare mutation of both and ) in primary astrocytic tumours
  publication-title: Br J Cancer
– volume: 48
  start-page: 5546
  year: 1988
  end-page: 5551
  article-title: Clonal genomic alterations in glioma malignancy stages
  publication-title: Cancer Res
– volume: 12
  start-page: 255
  year: 1995
  end-page: 261
  article-title: Two tumor suppressive loci on chromosome 10 involved in human glioblastomas
  publication-title: Genes Chromosomes Cancer
– volume: 58
  start-page: 1260
  year: 1996
  end-page: 1267
  article-title: Deletion mapping of gliomas suggests the presence of two small regions for candidate tumor‐suppressor genes in a 17‐cM interval on chromosome 10q
  publication-title: Am J Hum Genet
– volume: 87
  start-page: 363
  year: 1996
  end-page: 367
  article-title: Deletion mapping of chromosome 10 in human glioma
  publication-title: Jpn J Cancer Res
– volume: 49
  start-page: M218
  year: 1996
  end-page: M222
  article-title: Accumulation of allelic losses on chromosome 10 in human gliomas at recurrence
  publication-title: J Clin Pathol: Mol Pathol
– year: 1993
– volume: 7
  start-page: 173
  year: 1993
  end-page: 177
  article-title: Deletion mapping of the long arm of chromosome 10 in glioblastoma multiforme
  publication-title: Genes Chromosomes Cancer
– volume: 15
  start-page: 356
  year: 1997
  end-page: 362
  article-title: Identification of a candidate tumour suppressor gene, , at chromosome 10q23.3 that is mutated in multiple advanced cancers
  publication-title: Nat Genet
– volume: 34
  start-page: 250
  year: 1996
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB11
  publication-title: Genomics
  doi: 10.1006/geno.1996.0277
  contributor:
    fullname: Kimmelman
– volume: 13
  start-page: 1065
  year: 1996
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB8
  publication-title: Oncogene
  contributor:
    fullname: Ichimura
– volume-title: International histological classification of tumors
  year: 1993
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB12
  contributor:
    fullname: Kleihues
– volume: 7
  start-page: 173
  year: 1993
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB5
  publication-title: Genes Chromosomes Cancer
  doi: 10.1002/gcc.2870070311
  contributor:
    fullname: Fults
– volume: 5
  start-page: 75
  year: 1992
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB16
  publication-title: Genes Chromosomes Cancer
  doi: 10.1002/gcc.2870050111
  contributor:
    fullname: Rasheed
– volume: 275
  start-page: 1943
  year: 1997
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB13
  publication-title: Science
  doi: 10.1126/science.275.5308.1943
  contributor:
    fullname: Li
– volume: 26
  start-page: 239
  year: 1993
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB20
  publication-title: Int J Rad Oncol Biol Phys
  doi: 10.1016/0360-3016(93)90203-8
  contributor:
    fullname: Simpson
– volume: 11
  start-page: 210
  year: 1995
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB2
  publication-title: Nat Genet
  doi: 10.1038/ng1095-210
  contributor:
    fullname: Cairns
– volume: 92
  start-page: 169
  year: 1993
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB10
  publication-title: Hum Genet
  doi: 10.1007/BF00219686
  contributor:
    fullname: Karlbom
– volume: 87
  start-page: 363
  year: 1996
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB21
  publication-title: Jpn J Cancer Res
  doi: 10.1111/j.1349-7006.1996.tb00231.x
  contributor:
    fullname: Sonoda
– volume: 48
  start-page: 5546
  year: 1988
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB9
  publication-title: Cancer Res
  contributor:
    fullname: James
– volume: 10
  start-page: 2243
  year: 1995
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB17
  publication-title: Oncogene
  contributor:
    fullname: Rasheed
– volume: 53
  start-page: 5043
  year: 1993
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB14
  publication-title: Cancer Res
  contributor:
    fullname: Pershouse
– volume: 4
  start-page: 210
  year: 1989
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB4
  publication-title: Genomics
  doi: 10.1016/0888-7543(89)90302-9
  contributor:
    fullname: Fujimoto
– volume: 58
  start-page: 1260
  year: 1996
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB1
  publication-title: Am J Hum Genet
  contributor:
    fullname: Albarosa
– volume: 15
  start-page: 356
  year: 1997
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB23
  publication-title: Nat Genet
  doi: 10.1038/ng0497-356
  contributor:
    fullname: Steck
– volume: 49
  start-page: m218
  year: 1996
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB24
  publication-title: J Clin Pathol: Mol Pathol
  contributor:
    fullname: Tokiyoshi
– volume: 270
  start-page: 1945
  year: 1995
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB7
  publication-title: Science
  doi: 10.1126/science.270.5244.1945
  contributor:
    fullname: Hudson
– volume: 77
  start-page: 295
  year: 1992
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB25
  publication-title: J Neurosurg
  doi: 10.3171/jns.1992.77.2.0295
  contributor:
    fullname: von Deimling
– volume: 12
  start-page: 255
  year: 1995
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB22
  publication-title: Genes Chromosomes Cancer
  doi: 10.1002/gcc.2870120404
  contributor:
    fullname: Steck
– volume: 75
  start-page: 2
  year: 1997
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB19
  publication-title: Br J Cancer
  doi: 10.1038/bjc.1997.2
  contributor:
    fullname: Schmidt
– volume: 380
  start-page: 152
  year: 1996
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB3
  publication-title: Nature
  doi: 10.1038/380152a0
  contributor:
    fullname: Dib
– start-page: 83
  volume-title: Tumours of central neuroepithelial origin Pathology of Tumours of the Nervous System
  year: 1989
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB18
  contributor:
    fullname: Russell
– volume: 50
  start-page: 5784
  year: 1990
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB6
  publication-title: Cancer Res
  contributor:
    fullname: Fults
– volume: 5
  start-page: 357
  year: 1992
  ident: 10.1002/(SICI)1098-2264(199805)22:1<9::AID-GCC2>3.0.CO;2-1-BIB15
  publication-title: Genes Chromosomes Cancer
  doi: 10.1002/gcc.2870050412
  contributor:
    fullname: Ransom
SSID ssj0006395
Score 1.9418719
Snippet Deletions of chromosome 10 are the most frequent genetic abnormality in glioblastomas. Several commonly deleted regions have been proposed; however, they are...
SourceID proquest
crossref
pubmed
wiley
istex
SourceType Aggregation Database
Index Database
Publisher
StartPage 9
SubjectTerms Astrocytoma - genetics
Astrocytoma - pathology
Chromosome Deletion
Chromosomes, Human, Pair 10 - genetics
Genes, Tumor Suppressor - genetics
Glioblastoma - genetics
Glioblastoma - pathology
Humans
Microsatellite Repeats
Neoplasm Recurrence, Local
Title Distinct patterns of deletion on 10p and 10q suggest involvement of multiple tumor suppressor genes in the development of astrocytic gliomas of different malignancy grades
URI https://api.istex.fr/ark:/67375/WNG-J2JR1DR1-4/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2F%28SICI%291098-2264%28199805%2922%3A1%3C9%3A%3AAID-GCC2%3E3.0.CO%3B2-1
https://www.ncbi.nlm.nih.gov/pubmed/9591629
https://search.proquest.com/docview/79882817
Volume 22
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwxV1bb9MwFLamISZeuAwmytUPDG0P6RInTuKCkEa6S4u2SYVpe7N8azWNpaVJpZV_wm_gT3JO0osGE09ISJGSWq7PUc6x_Z34-DMhbywLeWihIxkthBdx4zxlVOi5VGullOHO4oru0XF8eBp1z_n5Crme74Wp-SEWH9ywZ1TjNXZwpYudJWkoALDPnawDAXOAnJi4IRSpjSB88DkUMoZkBJthJuAO126n7R1kGZTuhU2_mZ1shh-Zh3ETsvAhmuoteadg2uY1jQGHhnmyRlozwTtbKHR7IXKrFrjNWCt4L1qtuZgPtZB3IOLGjHcHjXd9G5y9iY6r6W3_AfkxfzF1Vstlc1Lqpvn-G2fk_3hzD8n9GWamu7WTPyIrLl8nd-tTNKfrZO1olh_wmPxs45CVm5KOKt7QvKDDPsWzftD_KFyBP6Iqt3D_RovJAFfX6EUOY3TFm15i9XmOJS0nV8Mx1BpVycLwOMCJAapTQM3ULtOt8F-qKAELTEFFOvh6gVlXlejZ-TMlvYKAZ4DsJlM6GCvriifkdH_vS3bozY6j8AwPI-ZFsVEO8LSfJiYKrdWAnIVirg-ouZ_YNI0joVPhYmsTJfBIE86iJHFxYJRQkQ43yGo-zN1TQpmxvlJJarlOI7SCH2vhm0S5ONHatw3yae4yclSzjsiaX5pJibbDxIFUouVkbTd4loEUUoK1JFpLhtKX2YmE4gZ5W3ndoik1vsR8voTLs-MD2WXdXtDuBTJqkNdzt5QwyuDSkcrdcFJIZLUDF0kaZKP21kVbgkOAwQRoXLncH-r-VdtblK1-P_unrT0n9-qdpJim-oKsluOJewlQstSvqm7_C5JBVrc
link.rule.ids 315,786,790,1382,27957,27958,46329,46753
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwxV3dT9swELcQaGwv-2BD677ww5jgISVx4iTupkksBdpCi1RA481yYrdCjLRrU2ndn7J_Yf_k7uJ-iA3tadKkSEkt13fKnc938fl3hLzVzOe-homUpUI4Ac-MozLlOyZOU6VUxo3GHd12J2xcBK1LfrlCpvOzMBYfYvHBDWdGaa9xguMH6b0laih4YGfNpAkRs4egmHgiFLGNIH5wOTQyhmgE234i4A7XfrPuHCUJtB74VbeanG77n5gDgdMa2ApeRmPdJfIULNzcAhlwGJlH66Q2o7y3g1R3FzR3LMVdxmreB1Grzel8tFTeA41ba94aiu_bXQ7tbf-4XOAOH5Ef81dj81quq5MirWbff0ON_C_v7jF5OHOb6b7V8ydkxeQb5J4tpDndIOvtWYrAU_KzjlYrzwo6LKFD8zEd9CiW-0EVpHB57pCqXMP9Kx1P-rjBRq9yMNMldHqB3edplrSY3AxG0GtY5gvDYx_XBuhOwXGmeplxhf9S4wLcgSmwSPtfrjDxqiQ9K0FT0BuIefoIcDKl_ZHSZvyMXBwenCcNZ1aRwsm4HzAnCDNlwKV24ygLfK1TcJ6FYqYHjnMv0nEcBiKNhQm1jpTAqiacBVFkQi9TQgWpv0lW80FunhPKMu0qFcWap3GAUnDDVLhZpEwYpamrK-R4rjNyaIFHpIWYZlKi7DB3IJYoOWnlBs_Sk0JKkJZEaUlfujI5ldBcIe9KtVsMpUbXmNIXcfm5cyRbrNX16l1PBhWyNddLCYYGd49UbgaTsURgO1CRqEI2rbouxhIcYgwmgONS5_5g96_c3sFs-fvFPx1ti9xvnLdP5Emzc_ySPLAHSzFr9RVZLUYT8xo8yyJ9U9qAXyWMWtk
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwxV1fb9MwELemTVS88GcwUf7NDwxtD-kSJ07igpBGum7tWIcGE3uz7NitprG0tKm08k34DHxJ7pKm1WDiCQkpUlLL9Z1y5_NdfP4dIa8M87lvYCKlWggn4Kl1VKp8x8ZaK6VSbg3u6B73wsOzoHvOz1fIdXUWpsSHWHxww5lR2Guc4CPT312ChoID9qmTdCBg9hATEw-EIrQRhA8uh0bGEIxgy08E3OHa67ScgySB1n2_4TaSky3_PXMgbloLQp_hfGidLoGnYN3mJY4Bh5F5VCPNOeXdbaS6s6C5XVLcYazpvRXNZkXnXUnlDdC4seStofSub_Nnb7rHxfrWvk9-VG-mTGu5bExz3Ui__wYa-T9e3QNyb-40071Syx-SFZutkztlGc3ZOqkdzxMEHpGfLbRZWZrTUQEcmk3osE-x2A8qIIXLc0dUZQbu3-hkOsDtNXqRgZEugNNz7F4lWdJ8ejUcQ69RkS0MjwNcGaA7BbeZmmW-Ff5LTXJwBmbAIh18vcC0q4L0vABNTq8g4hkgvMmMDsbK2Mljctbe_5wcOvN6FE7K_YA5QZgqCw61G0dp4BujwXUWitk-uM39yMRxGAgdCxsaEymBNU04C6LIhl6qhAq0v0FWs2FmnxDKUuMqFcWG6zhAKbihFm4aKRtGWrumTo4qlZGjEnZElgDTTEqUHWYOxBIlJ0u5wbP0pJASpCVRWtKXrkxOJDTXyetC6xZDqfElJvRFXH7pHcgu6556rVNPBnWyWamlBDODe0cqs8PpRCKsHahIVCcbpbYuxhIcIgwmgONC5f5g96_c3sJs8fvpPx1tk9Q-ttryQ6d39IzcLU-VYsrqc7Kaj6f2BbiVuX5ZWIBfoBBZiA
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=Distinct+patterns+of+deletion+on+10p+and+10q+suggest+involvement+of+multiple+tumor+suppressor+genes+in+the+development+of+astrocytic+gliomas+of+different+malignancy+grades&rft.jtitle=Genes+chromosomes+%26+cancer&rft.au=Ichimura%2C+K&rft.au=Schmidt%2C+E+E&rft.au=Miyakawa%2C+A&rft.au=Goike%2C+H+M&rft.date=1998-05-01&rft.issn=1045-2257&rft.volume=22&rft.issue=1&rft.spage=9&rft.epage=15&rft_id=info:doi/10.1002%2F%28SICI%291098-2264%28199805%2922%3A1%3C9%3A%3AAID-GCC2%3E3.0.CO%3B2-1&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1045-2257&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1045-2257&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1045-2257&client=summon