Results 61 to 70 of about 77,471 (339)
Background Fibro-adipose vascular anomaly (FAVA) is a rare and new entity of vascular anomaly. Activating mutations in the phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) gene were identified at a frequency of 62.5% in ...
Yumiko Hori +12 more
doaj +1 more source
Somatic MAP3K3 and PIK3CA mutations in sporadic cerebral and spinal cord cavernous malformations.
Cavernous malformations (CMs) affecting the central nervous system occur in approximately 0.16% to 0.4% of the general population. The majority (85%) of the CMs are in a sporadic form, but the genetic background of sporadic CMs remains enigmatic.
T. Hong +23 more
semanticscholar +1 more source
Transcriptional regulation of PIK3CA oncogene by NF-kappaB in ovarian cancer microenvironment. [PDF]
PIK3CA upregulation, amplification and mutation have been widely reported in ovarian cancers and other tumors, which strongly suggests that PIK3CA is a promising therapeutic target.
Nuo Yang +13 more
doaj +1 more source
The phosphatidylinositol 3-kinase (PI3K) pathway is an intracellular pathway activated in response to progrowth signaling, such as human epidermal growth factor receptor 2 (HER2) and other kinases.
Aryana R. Rasti +5 more
semanticscholar +1 more source
Relevance. The introduction of CDK4/6 inhibitors (palbociclib, ribociclib, and abemaciclib) into clinical practice has significantly improved the treatment outcomes of patients with metastatic HR+/HER2-breast cancer.
A. V. Fateeva +7 more
doaj +1 more source
Oncogenic activation of PIK3CA in cancers: Emerging targeted therapies in precision oncology
Phosphoinositide 3-kinases (PI3Ks) are heterodimers consisting of a p110 catalytic subunit and a p85 regulatory subunit. The PIK3CA gene, which encodes the p110α, is the most frequently mutated oncogene in cancer.
Yuxiang Wang +3 more
semanticscholar +1 more source
Somatic PIK3CA Mutations in Sporadic Cerebral Cavernous Malformations
BACKGROUND Cerebral cavernous malformations (CCMs) are common sporadic and inherited vascular malformations of the central nervous system. Although familial CCMs are linked to loss-of-function mutations in KRIT1 (CCM1), CCM2, or PDCD10 (CCM3), the ...
M. Peyre +19 more
semanticscholar +1 more source
Sequential targeting of the phosphatidylinositol 3-kinase (PI3K)/AKT pathway in hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer remains poorly described. We report a case of a 67-year-old woman
Han Yi Lee +2 more
doaj +1 more source
PIK3CA mutant tumors depend on oxoglutarate dehydrogenase [PDF]
Oncogenic PIK3CA mutations are found in a significant fraction of human cancers, but therapeutic inhibition of PI3K has only shown limited success in clinical trials.
Glenn S. Cowley +37 more
core +1 more source
Tumour heterogeneity and clonal evolution of metastatic salivary gland cancer were evaluated in two patients with adenoid carcinoma and one patient with myoepithelial carcinoma. Radiology‐guided autopsy enabled multi‐region sampling (total samples n = 149), followed by whole‐genome sequencing and phylogenetic reconstruction (17 tumour samples, 4–7 per ...
Gerben Lassche +10 more
wiley +1 more source

