#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Germline Variation Controls the Architecture of Somatic Alterations in Tumors


Studies have suggested that somatic events in tumors can depend on an individual's constitutional genotype. We used squamous cell carcinomas (SCC) of the skin, which arise in high multiplicity in organ transplant recipients, as a model to compare the pattern of somatic alterations within and across individuals. Specifically, we performed array comparative genomic hybridization on 104 tumors from 25 unrelated individuals who each had three or more independently arisen SCCs and compared the profiles occurring within patients to profiles of tumors across a larger set of 135 patients. In general, chromosomal aberrations in SCCs were more similar within than across individuals (two-sided exact-test p-value ), consistent with the notion that the genetic background was affecting the pattern of somatic changes. To further test this possibility, we performed allele-specific imbalance studies using microsatellite markers mapping to 14 frequently aberrant regions of multiple independent tumors from 65 patients. We identified nine loci which show evidence of preferential allelic imbalance. One of these loci, 8q24, corresponded to a region in which multiple single nucleotide polymorphisms have been associated with increased cancer risk in genome-wide association studies (GWAS). We tested three implicated variants and identified one, rs13281615, with evidence of allele-specific imbalance (p-value = 0.012). The finding of an independently identified cancer susceptibility allele with allele-specific imbalance in a genomic region affected by recurrent DNA copy number changes suggest that it may also harbor risk alleles for SCC. Together these data provide strong evidence that the genetic background is a key driver of somatic events in cancer, opening an opportunity to expand this approach to identify cancer risk alleles.


Vyšlo v časopise: Germline Variation Controls the Architecture of Somatic Alterations in Tumors. PLoS Genet 6(9): e32767. doi:10.1371/journal.pgen.1001136
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1001136

Souhrn

Studies have suggested that somatic events in tumors can depend on an individual's constitutional genotype. We used squamous cell carcinomas (SCC) of the skin, which arise in high multiplicity in organ transplant recipients, as a model to compare the pattern of somatic alterations within and across individuals. Specifically, we performed array comparative genomic hybridization on 104 tumors from 25 unrelated individuals who each had three or more independently arisen SCCs and compared the profiles occurring within patients to profiles of tumors across a larger set of 135 patients. In general, chromosomal aberrations in SCCs were more similar within than across individuals (two-sided exact-test p-value ), consistent with the notion that the genetic background was affecting the pattern of somatic changes. To further test this possibility, we performed allele-specific imbalance studies using microsatellite markers mapping to 14 frequently aberrant regions of multiple independent tumors from 65 patients. We identified nine loci which show evidence of preferential allelic imbalance. One of these loci, 8q24, corresponded to a region in which multiple single nucleotide polymorphisms have been associated with increased cancer risk in genome-wide association studies (GWAS). We tested three implicated variants and identified one, rs13281615, with evidence of allele-specific imbalance (p-value = 0.012). The finding of an independently identified cancer susceptibility allele with allele-specific imbalance in a genomic region affected by recurrent DNA copy number changes suggest that it may also harbor risk alleles for SCC. Together these data provide strong evidence that the genetic background is a key driver of somatic events in cancer, opening an opportunity to expand this approach to identify cancer risk alleles.


Zdroje

1. JonssonG

NaylorTL

Vallon-ChristerssonJ

StaafJ

HuangJ

2005 Distinct genomic profiles in hereditary breast tumors identified by array-based comparative genomic hybridization. Cancer Res 65 7612 7621

2. StefanssonOA

JonassonJG

JohannssonOT

OlafsdottirK

SteinarsdottirM

2009 Genomic profiling of breast tumours in relation to BRCA abnormalities and phenotypes. Breast Cancer Res 11 R47

3. LandiMT

BauerJ

PfeifferRM

ElderDE

HulleyB

2006 MC1R germline variants confer risk for BRAF-mutant melanoma. Science 313 521 522

4. MaldonadoJL

FridlyandJ

PatelH

JainAN

BusamK

2003 Determinants of BRAF mutations in primary melanomas. J Natl Cancer Inst 95 1878 1890

5. Ewart-TolandA

BriassouliP

de KoningJP

MaoJH

YuanJ

2003 Identification of Stk6/STK15 as a candidate low-penetrance tumor-susceptibility gene in mouse and human. Nat Genet 34 403 412

6. HienonenT

SalovaaraR

MecklinJP

JarvinenH

KarhuA

2006 Preferential amplification of AURKA 91A (Ile31) in familial colorectal cancers. Int J Cancer 118 505 508

7. RuivenkampCA

van WezelT

ZanonC

StassenAP

VlcekC

2002 Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancers. Nat Genet 31 295 300

8. TuupanenS

NiittymakiI

NousiainenK

VanharantaS

MecklinJP

2008 Allelic imbalance at rs6983267 suggests selection of the risk allele in somatic colorectal tumor evolution. Cancer Res 68 14 17

9. DiGiovannaJJ

1998 Posttransplantation skin cancer: scope of the problem, management, and role for systemic retinoid chemoprevention. Transplant Proc 30 2771 2775; discussion 2776–2778

10. AshtonKJ

WeinsteinSR

MaguireDJ

GriffithsLR

2003 Chromosomal aberrations in squamous cell carcinoma and solar keratoses revealed by comparative genomic hybridization. Arch Dermatol 139 876 882

11. PoppS

WalteringS

Holtgreve-GrezH

JauchA

ProbyC

2000 Genetic characterization of a human skin carcinoma progression model: from primary tumor to metastasis. J Invest Dermatol 115 1095 1103

12. MaoX

HamoudiRA

TalbotIC

BaudisM

2006 Allele-specific loss of heterozygosity in multiple colorectal adenomas: toward an integrated molecular cytogenetic map II. Cancer Genet Cytogenet 167 1 14

13. EastonDF

PooleyKA

DunningAM

PharoahPD

ThompsonD

2007 Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 447 1087 1093

14. FalchiM

BatailleV

HaywardNK

DuffyDL

BishopJA

2009 Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Nat Genet 41 915 919

15. TenesaA

FarringtonSM

PrendergastJG

PorteousME

WalkerM

2008 Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nat Genet 40 631 637

16. ChengI

PlummerSJ

JorgensonE

LiuX

RybickiBA

2008 8q24 and prostate cancer: association with advanced disease and meta-analysis. Eur J Hum Genet 16 496 505

17. FletcherO

JohnsonN

GibsonL

CouplandB

FraserA

2008 Association of genetic variants at 8q24 with breast cancer risk. Cancer Epidemiol Biomarkers Prev 17 702 705

18. Garcia-ClosasM

HallP

NevanlinnaH

PooleyK

MorrisonJ

2008 Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics. PLoS Genet 4 e1000054

19. LiL

PlummerSJ

ThompsonCL

MerkulovaA

AchesonLS

2008 A common 8q24 variant and the risk of colon cancer: a population-based case-control study. Cancer Epidemiol Biomarkers Prev 17 339 342

20. WokolorczykD

GliniewiczB

SikorskiA

ZlowockaE

MasojcB

2008 A range of cancers is associated with the rs6983267 marker on chromosome 8. Cancer Res 68 9982 9986

21. YeagerM

OrrN

HayesRB

JacobsKB

KraftP

2007 Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Nat Genet 39 645 649

22. GinzingerDG

GodfreyTE

NigroJ

MooreDH2nd

SuzukiS

2000 Measurement of DNA copy number at microsatellite loci using quantitative PCR analysis. Cancer Res 60 5405 5409

23. SnijdersAM

NoweeME

FridlyandJ

PiekJM

DorsmanJC

2003 Genome-wide-array-based comparative genomic hybridization reveals genetic homogeneity and frequent copy number increases encompassing CCNE1 in fallopian tube carcinoma. Oncogene 22 4281 4286

24. CurtinJA

FridlyandJ

KageshitaT

PatelHN

BusamKJ

2005 Distinct sets of genetic alterations in melanoma. N Engl J Med 353 2135 2147

25. R Development Core Team 2005 R: A Language and Environment for Statistical Computing Vienna, Austria R Foundation for Statistical Computing

26. GentlemanRC

CareyVJ

BatesDM

BolstadB

DettlingM

2004 Bioconductor: Open software development for computational biology and bioinformatics. Genome Biol 5 R80

27. GajduskovaP

SnijdersAM

KwekS

RoydasguptaR

FridlyandJ

2007 Genome position and gene amplification. Genome Biol 8 R120

28. OlshenAB

VenkatramanES

LucitoR

WiglerM

2004 Circular binary segmentation for the analysis of array-based DNA copy number data. Biostatistics 5 557 572

29. WillenbrockH

FridlyandJ

2005 A comparison study: applying segmentation to array CGH data for downstream analyses. Bioinformatics 21 4084 4091

30. BrownMB

ForsytheAB

1974 Robust tests for equality of variances. J Am Stat Assoc 69 364 367

31. WangC

HoriuchiA

ImaiT

OhiraS

ItohK

2004 Expression of BRCA1 protein in benign, borderline, and malignant epithelial ovarian neoplasms and its relationship to methylation and allelic loss of the BRCA1 gene. J Pathol 202 215 223

32. WeberF

ShenL

FukinoK

PatocsA

MutterGL

2006 Total-genome analysis of BRCA1/2-related invasive carcinomas of the breast identifies tumor stroma as potential landscaper for neoplastic initiation. Am J Hum Genet 78 961 972

33. van den BoomD

JurinkeC

McGinnissMJ

BerkenkampS

2001 Microsatellites: perspectives and potentials of mass spectrometric analysis. Expert Rev Mol Diagn 1 383 393

34. HaimanCA

Le MarchandL

YamamatoJ

StramDO

ShengX

2007 A common genetic risk factor for colorectal and prostate cancer. Nat Genet 39 954 956

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2010 Číslo 9
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#