Pregled bibliografske jedinice broj: 339420
PIK3CA and PTEN mutations in adenoid cystic carcinoma of the breast metastatic to kidney
PIK3CA and PTEN mutations in adenoid cystic carcinoma of the breast metastatic to kidney // Human pathology, 38 (2007), 9; 1425-1431 doi:10.1016/j.humpath.2007.03.021 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 339420 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
PIK3CA and PTEN mutations in adenoid cystic carcinoma of the breast metastatic to kidney
Autori
Vranić, Semir ; Bilalović, Nurija ; Lee, Lisa M.J. ; Krušlin, Božo ; Lilleberg, Stan L. ; Gatalica, Zoran
Izvornik
Human pathology (0046-8177) 38
(2007), 9;
1425-1431
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
adenoid cystic carcinoma ; breast ; mTOR ; PIK3CA ; PTEN
Sažetak
Adenoid cystic carcinoma (ACC) of the breast rarely metastasizes and has been associated with excellent prognosis. We describe a patient with renal metastasis of primary breast ACC 5 years after the mastectomy. A detailed molecular genetic analysis of the primary and metastatic tumors demonstrated somatic mutations in 2 well-known cancer genes associated with regulation of PI3K/AKT signaling pathway: (1) PIK3CA, which encodes the catalytic alpha subunit of the phosphoinositide-3-kinase, and (2) PTEN, which encodes phosphatase and tensin homolog. The mutation identified in PIK3CA (Ex1+169 A>C) predicts an amino acid change from isoleucine to methionine at codon 31 (I31M) and resides in the p85-binding domain of exon 1. The mutation identified in PTEN (IVS4-3 C>T) resides in intron 4 near the splice acceptor site of exon 5 and was associated with an aberrant PTEN transcript lacking exon 5, which is necessary for protein tyrosine phosphatase function and tumor suppressor properties of PTEN. Increased promoter methylation of PTEN was present in renal metastasis, coinciding with the decrease in the level of normal PTEN transcript. These coexistent mutations/epigenetic inactivations in PI3K/AKT pathway may be responsible for the unusually aggressive course of ACC.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
108-1081870-1884 - Razvojna neuropatologija genetskih malformacija moždane kore čovjeka (Krušlin, Božo, MZOS ) ( CroRIS)
134-0000000-3381 - Promjene bubrežne arterije u bolesnika s karcinomom bubrega (Čupić, Hrvoje, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb,
KBC "Sestre Milosrdnice"
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE