Akt kinases in breast cancer and the results of adjuvant therapy
- PMID: 12631397
- PMCID: PMC154147
- DOI: 10.1186/bcr569
Akt kinases in breast cancer and the results of adjuvant therapy
Abstract
Background: The serine/threonine kinase Akt, or protein kinase B, has recently been a focus of interest because of its activity to inhibit apoptosis. It mediates cell survival by acting as a transducer of signals from growth factor receptors that activate phosphatidylinositol 3-kinase.
Methods: We analysed the expression of the isoforms Akt1 and Akt2 as well as phosphorylated Akt (pAkt) by immunohistochemistry in frozen tumour samples from 280 postmenopausal patients who participated in a randomised trial comparing cyclophosphamide-methotrexate-5-fluorouracil chemotherapy and postoperative radiotherapy. The patients were simultaneously randomised to tamoxifen or to no endocrine treatment.
Results: Marked staining was found in 24% of the tumours for Akt1, but in only 4% for Akt2. A low frequency of Akt2-positive cells (1-10%) was observed in another 26% of the tumours. pAkt was significantly associated with both Akt1 and Akt2 expression. Overexpression of erbB2 correlated significantly with pAkt (P = 0.0028). The benefit from tamoxifen was analysed in oestrogen receptor (ER)-positive patients. Patients with a negative status of Akt (no overexpression of Akt1, Akt2 or pAkt) showed significant benefit from tamoxifen. The relative rate of distant recurrence, with versus without tamoxifen, was 0.44 (95% confidence interval [CI], 0.25-0.79) for ER+/Akt1- patients, while it was 0.72 (95% CI, 0.34-1.53) for ER+/Akt1+ patients. The difference in rate ratio did not reach statistical significance. The rate of locoregional recurrence was significantly decreased with radiotherapy versus chemotherapy for Akt-negative patients (rate ratio, 0.23; 95% CI, 0.08-0.67; P = 0.0074), while no benefit was evident for the Akt-positive subgroup (rate ratio, 0.77; 95% CI, 0.31-1.9; P = 0.58). The interaction between Akt and the efficacy of radiotherapy was significant in multivariate analysis (P = 0.042).
Conclusion: Activation of the Akt pathway is correlated with erbB2 overexpression in breast cancer. The results suggest that Akt may predict the local control benefit from radiotherapy.
Figures
Similar articles
-
AKT activation predicts outcome in breast cancer patients treated with tamoxifen.J Pathol. 2005 Oct;207(2):139-46. doi: 10.1002/path.1829. J Pathol. 2005. PMID: 16088978
-
Activation of AKT/PKB in breast cancer predicts a worse outcome among endocrine treated patients.Br J Cancer. 2002 Feb 12;86(4):540-5. doi: 10.1038/sj.bjc.6600126. Br J Cancer. 2002. PMID: 11870534 Free PMC article.
-
Adjuvant letrozole versus tamoxifen according to centrally-assessed ERBB2 status for postmenopausal women with endocrine-responsive early breast cancer: supplementary results from the BIG 1-98 randomised trial.Lancet Oncol. 2008 Jan;9(1):23-8. doi: 10.1016/S1470-2045(07)70386-8. Epub 2007 Dec 20. Lancet Oncol. 2008. PMID: 18083065 Clinical Trial.
-
ErbB (HER) receptors can abrogate antiestrogen action in human breast cancer by multiple signaling mechanisms.Clin Cancer Res. 2003 Jan;9(1 Pt 2):511S-5S. Clin Cancer Res. 2003. PMID: 12538508 Review.
-
LHRH agonists for adjuvant therapy of early breast cancer in premenopausal women.Cochrane Database Syst Rev. 2008 Oct 8;(4):CD004562. doi: 10.1002/14651858.CD004562.pub3. Cochrane Database Syst Rev. 2008. Update in: Cochrane Database Syst Rev. 2009 Oct 07;(4):CD004562. doi: 10.1002/14651858.CD004562.pub4 PMID: 18843661 Updated. Review.
Cited by
-
miR-600 inhibits lung cancer via downregulating the expression of METTL3.Cancer Manag Res. 2019 Feb 1;11:1177-1187. doi: 10.2147/CMAR.S181058. eCollection 2019. Cancer Manag Res. 2019. PMID: 30774445 Free PMC article.
-
New insights on PI3K/AKT pathway alterations and clinical outcomes in breast cancer.Cancer Treat Rev. 2016 Apr;45:87-96. doi: 10.1016/j.ctrv.2016.03.004. Epub 2016 Mar 9. Cancer Treat Rev. 2016. PMID: 26995633 Free PMC article. Review.
-
Detection of pAkt protein in imprint cytology of invasive breast cancer: Correlation with HER2/neu, hormone receptors, and other clinicopathological variables.Cytojournal. 2015 Mar 25;12:6. doi: 10.4103/1742-6413.153965. eCollection 2015. Cytojournal. 2015. PMID: 25838835 Free PMC article.
-
Alpha-actinin 4 and tumorigenesis of breast cancer.Vitam Horm. 2013;93:323-51. doi: 10.1016/B978-0-12-416673-8.00005-8. Vitam Horm. 2013. PMID: 23810014 Free PMC article. Review.
-
p-AKT overexpression in primary renal cell carcinomas and their metastases.Clin Exp Metastasis. 2010 Dec;27(8):611-7. doi: 10.1007/s10585-010-9351-y. Epub 2010 Sep 16. Clin Exp Metastasis. 2010. PMID: 20844931
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous