The branched-chain amino acid transaminase 1 sustains growth of antiestrogen-resistant and ERα-negative breast cancer
Antiestrogen-resistant and triple-negative breast tumors pose a serious clinical challenge because of limited treatment options. We assessed global gene expression changes in antiestrogen-sensitive compared with antiestrogen-resistant (two tamoxifen resistant and two fulvestrant resistant) MCF-7 bre...
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| Hauptverfasser: | , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
20 March 2017
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| In: |
Oncogene
Year: 2017, Jahrgang: 36, Heft: 29, Pages: 4124-4134 |
| ISSN: | 1476-5594 |
| DOI: | 10.1038/onc.2017.32 |
| Online-Zugang: | Verlag, Pay-per-use, Volltext: http://dx.doi.org/10.1038/onc.2017.32 Verlag, Pay-per-use, Volltext: https://www.nature.com/articles/onc201732 
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| Verfasserangaben: | V. Thewes, R. Simon, M. Hlevnjak, M. Schlotter, P. Schroeter, K. Schmidt, Y. Wu, T. Anzeneder, W. Wang, P. Windisch, M. Kirchgäßner, N. Melling, N. Kneisel, R. Büttner, U. Deuschle, H.P. Sinn, A. Schneeweiss, S. Heck, S. Kaulfuss, H. Hess-Stumpp, J.G. Okun, G. Sauter, A.E. Lykkesfeldt, M. Zapatka, B. Radlwimmer, P. Lichter & M. Tönjes |
MARC
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| 245 | 1 | 4 | |a The branched-chain amino acid transaminase 1 sustains growth of antiestrogen-resistant and ERα-negative breast cancer |c V. Thewes, R. Simon, M. Hlevnjak, M. Schlotter, P. Schroeter, K. Schmidt, Y. Wu, T. Anzeneder, W. Wang, P. Windisch, M. Kirchgäßner, N. Melling, N. Kneisel, R. Büttner, U. Deuschle, H.P. Sinn, A. Schneeweiss, S. Heck, S. Kaulfuss, H. Hess-Stumpp, J.G. Okun, G. Sauter, A.E. Lykkesfeldt, M. Zapatka, B. Radlwimmer, P. Lichter & M. Tönjes |
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| 520 | |a Antiestrogen-resistant and triple-negative breast tumors pose a serious clinical challenge because of limited treatment options. We assessed global gene expression changes in antiestrogen-sensitive compared with antiestrogen-resistant (two tamoxifen resistant and two fulvestrant resistant) MCF-7 breast cancer cell lines. The branched-chain amino acid transaminase 1 (BCAT1), which catalyzes the first step in the breakdown of branched-chain amino acids, was among the most upregulated transcripts in antiestrogen-resistant cells. Elevated BCAT1 expression was confirmed in relapsed tamoxifen-resistant breast tumor specimens. High intratumoral BCAT1 levels were associated with a reduced relapse-free survival in adjuvant tamoxifen-treated patients and overall survival in unselected patients. On a tissue microarray (n=1421), BCAT1 expression was detectable in 58% of unselected primary breast carcinomas and linked to a higher Ki-67 proliferation index, as well as histological grade. Interestingly, BCAT1 was predominantly expressed in estrogen receptor-α-negative/human epidermal growth factor receptor-2-positive (ERα-negative/HER-2-positive) and triple-negative breast cancers in independent patient cohorts. The inverse relationship between BCAT1 and ERα was corroborated in various breast cancer cell lines and pharmacological long-term depletion of ERα induced BCAT1 expression in vitro. Mechanistically, BCAT1 indirectly controlled expression of the cell cycle inhibitor p27Kip1 thereby affecting pRB. Correspondingly, phenotypic analyses using a lentiviral-mediated BCAT1 short hairpin RNA knockdown revealed that BCAT1 sustains proliferation in addition to migration and invasion and that its overexpression enhanced the capacity of antiestrogen-sensitive cells to grow in the presence of antiestrogens. Importantly, silencing of BCAT1 in an orthotopic triple-negative xenograft model resulted in a massive reduction of tumor volume in vivo, supporting our findings that BCAT1 is necessary for the growth of hormone-independent breast tumors. | ||
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