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The prognostic value of PI3K mutational status in breast cancer: A meta-analysis.
- Source :
-
Journal of cellular biochemistry [J Cell Biochem] 2018 Jun; Vol. 119 (6), pp. 4287-4292. Date of Electronic Publication: 2018 Mar 01. - Publication Year :
- 2018
-
Abstract
- Breast cancer (BC) is the second most common cause of cancer-related deaths in women worldwide. The availability of reliable biomarkers of response/resistance to cancer treatments would benefit patients and clinicians allowing for a better selection of BC patients most likely to respond to a specific treatment. Phosphatidylinositol 3-kinase (PI3K) enzymes are involved in numerous cellular- functions and processes. The gene encoding for PI3K catalytic subunit p110α is mutated in 20-40% of BC. We performed a meta-analysis of the current literature on randomized clinical trials, investigating the role of PIK3CA mutational status as prognostic factor, and predictor of response to anti-cancer treatments. Overall 1929 cases were included. The pooled analysis confirmed that the presence of a PIK3CA mutation represents an independent negative prognostic factor (HR = 1.67, 95%CI: 1.15-2.43; P = 0.007) in BC, as previously reported. As PI3K signaling is also a result of other pathways' hyperactivation, further investigation of potential biomarkers able to predict likelihood of response to anti-PI3K/mTOR, anti-HER2, and other TKRs is warranted in future randomized clinical trials.<br /> (© 2018 Wiley Periodicals, Inc.)
- Subjects :
- Breast Neoplasms diagnosis
Breast Neoplasms enzymology
Breast Neoplasms therapy
Class I Phosphatidylinositol 3-Kinases metabolism
Female
Humans
Neoplasm Proteins metabolism
Prognosis
Breast Neoplasms genetics
Class I Phosphatidylinositol 3-Kinases genetics
Neoplasm Proteins genetics
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4644
- Volume :
- 119
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of cellular biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 29345357
- Full Text :
- https://doi.org/10.1002/jcb.26687