Is Co-Expressed with Closely Adjacent Uncharacterised Genes Spanning a Breast Cancer Susceptibility Locus at 6q25.1
Approximately 80% of human breast carcinomas present as oestrogen receptor α-positive (ER+ve) disease, and ER status is a critical factor in treatment decision-making. Recently, single nucleotide polymorphisms (SNPs) in the region immediately upstream of the ER gene (ESR1) on 6q25.1 have been associated with breast cancer risk. Our investigation of factors associated with the level of expression of ESR1 in ER+ve tumours has revealed unexpected associations between genes in this region and ESR1 expression that are important to consider in studies of the genetic causes of breast cancer risk. RNA from tumour biopsies taken from 104 postmenopausal women before and after 2 weeks treatment with an aromatase (oestrogen synthase) inhibitor was analyzed on Illumina 48K microarrays. Multiple-testing corrected Spearman correlation revealed that three previously uncharacterized open reading frames (ORFs) located immediately upstream of ESR1, C6ORF96, C6ORF97, and C6ORF211 were highly correlated with ESR1 (Rs = 0.67, 0.64, and 0.55 respectively, FDR<1×10−7). Publicly available datasets confirmed this relationship in other groups of ER+ve tumours. DNA copy number changes did not account for the correlations. The correlations were maintained in cultured cells. An ERα antagonist did not affect the ORFs' expression or their correlation with ESR1, suggesting their transcriptional co-activation is not directly mediated by ERα. siRNA inhibition of C6ORF211 suppressed proliferation in MCF7 cells, and C6ORF211 positively correlated with a proliferation metagene in tumours. In contrast, C6ORF97 expression correlated negatively with the metagene and predicted for improved disease-free survival in a tamoxifen-treated published dataset, independently of ESR1. Our observations suggest that some of the biological effects previously attributed to ER could be mediated and/or modified by these co-expressed genes. The co-expression and function of these genes may be important influences on the recently identified relationship between SNPs in this region and breast cancer risk.
Vyšlo v časopise:
Is Co-Expressed with Closely Adjacent Uncharacterised Genes Spanning a Breast Cancer Susceptibility Locus at 6q25.1. PLoS Genet 7(4): e32767. doi:10.1371/journal.pgen.1001382
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1001382
Souhrn
Approximately 80% of human breast carcinomas present as oestrogen receptor α-positive (ER+ve) disease, and ER status is a critical factor in treatment decision-making. Recently, single nucleotide polymorphisms (SNPs) in the region immediately upstream of the ER gene (ESR1) on 6q25.1 have been associated with breast cancer risk. Our investigation of factors associated with the level of expression of ESR1 in ER+ve tumours has revealed unexpected associations between genes in this region and ESR1 expression that are important to consider in studies of the genetic causes of breast cancer risk. RNA from tumour biopsies taken from 104 postmenopausal women before and after 2 weeks treatment with an aromatase (oestrogen synthase) inhibitor was analyzed on Illumina 48K microarrays. Multiple-testing corrected Spearman correlation revealed that three previously uncharacterized open reading frames (ORFs) located immediately upstream of ESR1, C6ORF96, C6ORF97, and C6ORF211 were highly correlated with ESR1 (Rs = 0.67, 0.64, and 0.55 respectively, FDR<1×10−7). Publicly available datasets confirmed this relationship in other groups of ER+ve tumours. DNA copy number changes did not account for the correlations. The correlations were maintained in cultured cells. An ERα antagonist did not affect the ORFs' expression or their correlation with ESR1, suggesting their transcriptional co-activation is not directly mediated by ERα. siRNA inhibition of C6ORF211 suppressed proliferation in MCF7 cells, and C6ORF211 positively correlated with a proliferation metagene in tumours. In contrast, C6ORF97 expression correlated negatively with the metagene and predicted for improved disease-free survival in a tamoxifen-treated published dataset, independently of ESR1. Our observations suggest that some of the biological effects previously attributed to ER could be mediated and/or modified by these co-expressed genes. The co-expression and function of these genes may be important influences on the recently identified relationship between SNPs in this region and breast cancer risk.
Zdroje
1. ParkinDM
BrayF
FerlayJ
PisaniP
2005 Global cancer statistics, 2002. CA Cancer J Clin 55 74 108
2. DowsettM
DunbierAK
2008 Emerging biomarkers and new understanding of traditional markers in personalized therapy for breast cancer. Clin Cancer Res 14 8019 8026
3. PerouCM
SorlieT
EisenMB
van de RijnM
JeffreySS
2000 Molecular portraits of human breast tumours. Nature 406 747 752
4. HammesSR
LevinER
2007 Extranuclear steroid receptors: nature and actions. Endocr Rev 28 726 741
5. SorlieT
TibshiraniR
ParkerJ
HastieT
MarronJS
2003 Repeated observation of breast tumor subtypes in independent gene expression data sets. Proc Natl Acad Sci U S A 100 8418 8423
6. ZhengW
LongJ
GaoYT
LiC
ZhengY
2009 Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. Nat Genet 41 324 328
7. TurnbullC
AhmedS
MorrisonJ
PernetD
RenwickA
2010 Genome-wide association study identifies five new breast cancer susceptibility loci. Nat Genet 42 504 7
8. StaceySN
SulemP
ZanonC
GudjonssonSA
ThorleifssonG
2010 Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus. PLoS Genet 6 e1001029 doi:10.1371/journal.pgen.1001029
9. FletcherO
JohnsonN
OrrN
HoskingFJ
GibsonLJ
2011 Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study. J Natl Cancer Inst 103 425 35
10. CaiQ
WenW
QuS
LiG
EganKM
2011 Replication and Functional Genomic Analyses of the Breast Cancer Susceptibility Locus at 6q25.1 Generalize Its Importance in Women of Chinese, Japanese, and European Ancestry. Cancer Res 71 1344 1355
11. FrasorJ
DanesJM
KommB
ChangKC
LyttleCR
2003 Profiling of estrogen up- and down-regulated gene expression in human breast cancer cells: insights into gene networks and pathways underlying estrogenic control of proliferation and cell phenotype. Endocrinology 144 4562 4574
12. OhDS
TroesterMA
UsaryJ
HuZ
HeX
2006 Estrogen-regulated genes predict survival in hormone receptor-positive breast cancers. J Clin Oncol 24 1656 1664
13. YuJ
YuJ
CorderoKE
JohnsonMD
GhoshD
2008 A transcriptional fingerprint of estrogen in human breast cancer predicts patient survival. Neoplasia 10 79 88
14. MillerWR
LarionovAA
RenshawL
AndersonTJ
WhiteS
2007 Changes in breast cancer transcriptional profiles after treatment with the aromatase inhibitor, letrozole. Pharmacogenet Genomics 17 813 826
15. MackayA
UrruticoecheaA
DixonJM
DexterT
FenwickK
2007 Molecular response to aromatase inhibitor treatment in primary breast cancer. Breast Cancer Res 9 R37
16. Mello-GrandM
SinghV
GhimentiC
ScatoliniM
RegoloL
2010 Gene expression profiling and prediction of response to hormonal neoadjuvant treatment with anastrozole in surgically resectable breast cancer. Breast Cancer Res Treat
17. CarrollJS
MeyerCA
SongJ
LiW
GeistlingerTR
2006 Genome-wide analysis of estrogen receptor binding sites. Nat Genet 38 1289 1297
18. FullwoodMJ
LiuMH
PanYF
LiuJ
XuH
2009 An oestrogen-receptor-alpha-bound human chromatin interactome. Nature 462 58 64
19. RaeJM
JohnsonMD
ScheysJO
CorderoKE
LariosJM
2005 GREB 1 is a critical regulator of hormone dependent breast cancer growth. Breast Cancer Res Treat 92 141 149
20. ShangY
HuX
DiRenzoJ
LazarMA
BrownM
2000 Cofactor dynamics and sufficiency in estrogen receptor-regulated transcription. Cell 103 843 852
21. MusgroveEA
SutherlandRL
2009 Biological determinants of endocrine resistance in breast cancer. Nat Rev Cancer 9 631 643
22. AliS
CoombesRC
2002 Endocrine-responsive breast cancer and strategies for combating resistance. Nat Rev Cancer 2 101 112
23. SmithIE
WalshG
SkeneA
LlombartA
MayordomoJI
2007 A phase II placebo-controlled trial of neoadjuvant anastrozole alone or with gefitinib in early breast cancer. J Clin Oncol 25 3816 3822
24. WangY
KlijnJG
ZhangY
SieuwertsAM
LookMP
2005 Gene-expression profiles to predict distant metastasis of lymph-node-negative primary breast cancer. Lancet 365 671 679
25. HolstF
StahlPR
RuizC
HellwinkelO
JehanZ
2007 Estrogen receptor alpha (ESR1) gene amplification is frequent in breast cancer. Nat Genet 39 655 660
26. Reis-FilhoJS
DruryS
LambrosMB
MarchioC
JohnsonN
2008 ESR1 gene amplification in breast cancer: a common phenomenon? Nat Genet 40 809 810; author reply 810-802
27. MackayA
TamberN
FenwickK
IravaniM
GrigoriadisA
2009 A high-resolution integrated analysis of genetic and expression profiles of breast cancer cell lines. Breast Cancer Res Treat 118 481 498
28. XiaW
BacusS
HegdeP
HusainI
StrumJ
2006 A model of acquired autoresistance to a potent ErbB2 tyrosine kinase inhibitor and a therapeutic strategy to prevent its onset in breast cancer. Proc Natl Acad Sci U S A 103 7795 7800
29. LearyAF
MartinL
ThornhillA
DowsettM
JohnstonS
2010 Combining or Sequencing Targeted Therapies in ER+/HER2 Amplified Breast Cancer (BC): In Vitro and In Vivo Studies of Letrozole and Lapatinib in an ER+/HER2+ Aromatase-Transfected BC Model. Cancer Res 70 292s
30. MartinLA
FarmerI
JohnstonSR
AliS
MarshallC
2003 Enhanced estrogen receptor (ER) alpha, ERBB2, and MAPK signal transduction pathways operate during the adaptation of MCF-7 cells to long term estrogen deprivation. J Biol Chem 278 30458 30468
31. WakelingAE
BowlerJ
1992 ICI 182,780, a new antioestrogen with clinical potential. J Steroid Biochem Mol Biol 43 173 177
32. McClellandRA
GeeJM
FrancisAB
RobertsonJF
BlameyRW
1996 Short-term effects of pure anti-oestrogen ICI 182780 treatment on oestrogen receptor, epidermal growth factor receptor and transforming growth factor-alpha protein expression in human breast cancer. Eur J Cancer 32A 413 416
33. LiGJ
ZhaoQ
ZhengW
2005 Alteration at translational but not transcriptional level of transferrin receptor expression following manganese exposure at the blood-CSF barrier in vitro. Toxicol Appl Pharmacol 205 188 200
34. GhazouiZ
BuffaFM
DunbierAK
AndersonH
DexterT
2011 Close and stable relationship between proliferation and a hypoxia metagene in aromatase inhibitor treated ER-positive breast cancer. Clin Cancer Res
35. LoiS
Haibe-KainsB
DesmedtC
WirapatiP
LallemandF
2008 Predicting prognosis using molecular profiling in estrogen receptor-positive breast cancer treated with tamoxifen. BMC Genomics 9 239
36. LoiS
Haibe-KainsB
DesmedtC
LallemandF
TuttAM
2007 Definition of clinically distinct molecular subtypes in estrogen receptor-positive breast carcinomas through genomic grade. J Clin Oncol 25 1239 1246
37. DruryS
JohnsonN
HillsM
SalterJ
DunbierA
2010 A breast cancer-associated SNP adjacent to ESR1 correlates with oestrogen receptor-alpha (ER alpha) level in invasive breast tumours. Cancer Res 69 4138
38. DunbierAK
AndersonH
GhazouiZ
PancholiS
SidhuK
2010 ESR1 is co-expressed with closely adjacent novel genes in estrogen receptor positive breast cancer. Presented at the 101st American Association for Cancer Research Annual Meeting, Washington DC, USA Abstract number 2916
39. LazennecG
HuignardH
ValotaireY
KernL
1995 Characterization of the transcription start point of the trout estrogen receptor-encoding gene: evidence for alternative splicing in the 5′ untranslated region. Gene 166 243 247
40. MartinMB
SacedaM
Garcia-MoralesP
GottardisMM
1994 Regulation of estrogen receptor expression. Breast Cancer Res Treat 31 183 189
41. MartinMB
AngeloniSV
Garcia-MoralesP
ShollerPF
Castro-GalacheMD
2004 Regulation of estrogen receptor-alpha expression in MCF-7 cells by taxol. J Endocrinol 180 487 496
42. AngeloniSV
MartinMB
Garcia-MoralesP
Castro-GalacheMD
FerragutJA
2004 Regulation of estrogen receptor-alpha expression by the tumor suppressor gene p53 in MCF-7 cells. J Endocrinol 180 497 504
43. Lieberman-AidenE
van BerkumNL
WilliamsL
ImakaevM
RagoczyT
2009 Comprehensive mapping of long-range interactions reveals folding principles of the human genome. Science 326 289 293
44. http://www.genecards.org/
45. http://www.ncbi.nlm.nih.gov/homologene
46. EwingRM
ChuP
ElismaF
LiH
TaylorP
2007 Large-scale mapping of human protein-protein interactions by mass spectrometry. Mol Syst Biol 3 89
47. Early Breast Cancer Trialists' Collaborative Group 1998 Tamoxifen for early breast cancer: an overview of the randomised trials. Lancet 351 1451 1467
48. The World Medical Association: Declaration of Helsinki. http://www.wma.net/e/policy/b3htm
49. DuP
KibbeWA
LinSM
2008 lumi: a pipeline for processing Illumina microarray. Bioinformatics 24 1547 1548
50. KornEL
TroendleJF
McShaneLM
SimonR
2004 Controlling the number of false discoveries: application to high-dimensional genomic data. Journal of Statistical Planning and Inference 124 379 398
51. MillerLD
SmedsJ
GeorgeJ
VegaVB
VergaraL
2005 An expression signature for p53 status in human breast cancer predicts mutation status, transcriptional effects, and patient survival. Proc Natl Acad Sci U S A 102 13550 13555
52. DesmedtC
PietteF
LoiS
WangY
LallemandF
2007 Strong time dependence of the 76-gene prognostic signature for node-negative breast cancer patients in the TRANSBIG multicenter independent validation series. Clin Cancer Res 13 3207 3214
53. HuangF
ReevesK
HanX
FairchildC
PlateroS
2007 Identification of candidate molecular markers predicting sensitivity in solid tumors to dasatinib: rationale for patient selection. Cancer Res 67 2226 2238
54. GhazouiZ
BuffaFM
DunbierAK
AndersonH
DexterT
2009 Aromatase Inhibitors Reduce the Expression of a Hypoxia Metagene in Oestrogen Receptor Positive Breast Cancer in Postmenopausal Women. Cancer Res 69 408
55. MarchioC
IravaniM
NatrajanR
LambrosMB
SavageK
2008 Genomic and immunophenotypical characterization of pure micropapillary carcinomas of the breast. J Pathol 215 398 410
56. NatrajanR
WeigeltB
MackayA
GeyerFC
GrigoriadisA
2010 An integrative genomic and transcriptomic analysis reveals molecular pathways and networks regulated by copy number aberrations in basal-like, HER2 and luminal cancers. Breast Cancer Res Treat 121 575 589
57. DruryS
AndersonH
DowsettM
2009 Selection of REFERENCE genes for normalization of qRT-PCR data derived from FFPE breast tumors. Diagn Mol Pathol 18 103 107
58. PancholiS
LykkesfeldtAE
HilmiC
BanerjeeS
LearyA
2008 ERBB2 influences the subcellular localization of the estrogen receptor in tamoxifen-resistant MCF-7 cells leading to the activation of AKT and RPS6KA2. Endocr Relat Cancer 15 985 1002
59. DarbreP
YatesJ
CurtisS
KingRJ
1983 Effect of estradiol on human breast cancer cells in culture. Cancer Res 43 349 354
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