Triple-negative breast cancer (TNBC) is characterised by poor outcomes and a historical lack of targeted therapies. Dysregulation of signalling through the phosphoinositide 3 (PI3) …
Since its discovery as the elusive tumor suppressor gene at the frequently mutated 10q23 locus, PTEN has been identified as lost or mutated in several sporadic and heritable tumor …
K Podsypanina, LH Ellenson… - Proceedings of the …, 1999 - National Acad Sciences
Pten/Mmac1+/− heterozygous mice exhibited neoplasms in multiple organs including the endometrium, liver, prostate, gastrointestinal tract, thyroid, and thymus. Loss of the wild-type …
C Eng - Human mutation, 2003 - Wiley Online Library
Abstract PTEN, on 10q23. 3, encodes a major lipid phosphatase which signals down the phosphoinositol‐3‐kinase/Akt pathway and effects G1 cell cycle arrest and apoptosis …
L Simpson, R Parsons - Experimental cell research, 2001 - Elsevier
PTEN, a tumor suppressor located at chromosome 10q23, is mutated in a variety of sporadic cancers and in two autosomal dominant hamartoma syndromes. PTEN is a phosphatase …
IU Ali, LM Schriml, M Dean - Journal of the national cancer …, 1999 - academic.oup.com
Abstract PTEN/MMAC1 (phosphatase, tensin homologue/mutated in multiple advanced cancers) is a tumor suppressor protein that has sequence homology with dual-specificity …
The PTEN tumor suppressor was discovered by its homozygous deletion and other mutations in cancer. Since then, PTEN has been shown to be a non-redundant …
PL Depowski, SI Rosenthal, JS Ross - Modern Pathology, 2001 - Elsevier
Introduction: The PTEN gene, a candidate tumor suppressor, is localized to chromosome 10q23 and shares extensive homology with cytoskeletal proteins auxilin and tensin. A high …
A Perren, LP Weng, AH Boag, U Ziebold… - The American journal of …, 1999 - Elsevier
Germline mutations in PTEN, encoding a dual-specificity phosphatase on 10q23. 3, cause Cowden syndrome (CS), which is characterized by a high risk of breast and thyroid cancers …