» Articles » PMID: 16670003

AIB1 Gene Amplification and the Instability of PolyQ Encoding Sequence in Breast Cancer Cell Lines

Overview
Journal BMC Cancer
Publisher Biomed Central
Specialty Oncology
Date 2006 May 4
PMID 16670003
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The poly Q polymorphism in AIB1 (amplified in breast cancer) gene is usually assessed by fragment length analysis which does not reveal the actual sequence variation. The purpose of this study is to investigate the sequence variation of poly Q encoding region in breast cancer cell lines at single molecule level, and to determine if the sequence variation is related to AIB1 gene amplification.

Methods: The polymorphic poly Q encoding region of AIB1 gene was investigated at the single molecule level by PCR cloning/sequencing. The amplification of AIB1 gene in various breast cancer cell lines were studied by real-time quantitative PCR.

Results: Significant amplifications (5-23 folds) of AIB1 gene were found in 2 out of 9 (22%) ER positive cell lines (in BT-474 and MCF-7 but not in BT-20, ZR-75-1, T47D, BT483, MDA-MB-361, MDA-MB-468 and MDA-MB-330). The AIB1 gene was not amplified in any of the ER negative cell lines. Different passages of MCF-7 cell lines and their derivatives maintained the feature of AIB1 amplification. When the cells were selected for hormone independence (LCC1) and resistance to 4-hydroxy tamoxifen (4-OH TAM) (LCC2 and R27), ICI 182,780 (LCC9) or 4-OH TAM, KEO and LY 117018 (LY-2), AIB1 copy number decreased but still remained highly amplified. Sequencing analysis of poly Q encoding region of AIB1 gene did not reveal specific patterns that could be correlated with AIB1 gene amplification. However, about 72% of the breast cancer cell lines had at least one under represented (<20%) extra poly Q encoding sequence patterns that were derived from the original allele, presumably due to somatic instability. Although all MCF-7 cells and their variants had the same predominant poly Q encoding sequence pattern of (CAG)3CAA(CAG)9(CAACAG)3(CAACAGCAG)2CAA of the original cell line, a number of altered poly Q encoding sequences were found in the derivatives of MCF-7 cell lines.

Conclusion: These data suggest that poly Q encoding region of AIB1 gene is somatic unstable in breast cancer cell lines. The instability and the sequence characteristics, however, do not appear to be associated with the level of the gene amplification.

Citing Articles

Targeting the IL-6/STAT3 Signalling Cascade to Reverse Tamoxifen Resistance in Estrogen Receptor Positive Breast Cancer.

Tsoi H, Man E, Chau K, Khoo U Cancers (Basel). 2021; 13(7).

PMID: 33806019 PMC: 8036560. DOI: 10.3390/cancers13071511.


Intrinsically Disordered SRC-3/AIB1 Protein Undergoes Homeostatic Nuclear Extrusion by Nuclear Budding While Ectopic Expression Induces Nucleophagy.

Cabrita M, Renart L, Lau R, Pratt M Cells. 2019; 8(10).

PMID: 31635050 PMC: 6830083. DOI: 10.3390/cells8101278.


BQ323636.1, a Novel Splice Variant to 2, as a Predictor for Tamoxifen-Resistant Breast Cancer.

Gong C, Man E, Tsoi H, Lee T, Lee P, Ma S Clin Cancer Res. 2018; 24(15):3681-3691.

PMID: 29420220 PMC: 6038915. DOI: 10.1158/1078-0432.CCR-17-2259.


Molecular-genetic profiling and high-throughput drug screening in NUT midline carcinoma-an aggressive and fatal disease.

Stirnweiss A, Oommen J, Kotecha R, Kees U, Beesley A Oncotarget. 2018; 8(68):112313-112329.

PMID: 29348827 PMC: 5762512. DOI: 10.18632/oncotarget.22862.


Chaperonin CCT-mediated AIB1 folding promotes the growth of ERα-positive breast cancer cells on hard substrates.

Chen L, Zhang Z, Qiu J, Zhang L, Luo X, Jang J PLoS One. 2014; 9(5):e96085.

PMID: 24788909 PMC: 4006900. DOI: 10.1371/journal.pone.0096085.


References
1.
Reiter R, Wellstein A, Riegel A . An isoform of the coactivator AIB1 that increases hormone and growth factor sensitivity is overexpressed in breast cancer. J Biol Chem. 2001; 276(43):39736-41. DOI: 10.1074/jbc.M104744200. View

2.
Kallioniemi A, Kallioniemi O, Piper J, Tanner M, Stokke T, Chen L . Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization. Proc Natl Acad Sci U S A. 1994; 91(6):2156-60. PMC: 43329. DOI: 10.1073/pnas.91.6.2156. View

3.
Shibata A, Hayashi Y, Imai T, Funahashi H, Nakao A, Seo H . Somatic gene alteration of AIB1 gene in patients with breast cancer. Endocr J. 2001; 48(2):199-204. DOI: 10.1507/endocrj.48.199. View

4.
Glaeser M, Floetotto T, Hanstein B, Beckmann M, Niederacher D . Gene amplification and expression of the steroid receptor coactivator SRC3 (AIB1) in sporadic breast and endometrial carcinomas. Horm Metab Res. 2001; 33(3):121-6. DOI: 10.1055/s-2001-14938. View

5.
Zeillinger R, Kury F, Czerwenka K, Kubista E, Sliutz G, Knogler W . HER-2 amplification, steroid receptors and epidermal growth factor receptor in primary breast cancer. Oncogene. 1989; 4(1):109-14. View