| Literature DB >> 27157405 |
Mounia Chidiac1, Mohammad Fayyad-Kazan2, Jalil Daher2, Philippe Poelvoorde2, Isabelle Bar3, Carine Maenhaut4, Paul Delrée5, Bassam Badran6, Luc Vanhamme7.
Abstract
The apolipoprotein L (apoL) family has not yet been ascribed any definite patho-physiological function although the conserved BH3 protein domain suggests a role in programmed cell death. As repression of the regular apoptotic program is considered a hallmark of tumor progression, we investigated apoL expression in cancer. We show that the levels of one member of the family, apolipoprotein L1 (apoL1) is higher in papillary thyroid carcinoma compared to normal tissue. A combination of qRTPCR, immunohistochemistry and in situ hybridization allowed us to ascribe this increase to endogenous overexpression in carcinoma cells. Whether apoL1 plays an instrumental role in refraining cell death is the subject of ongoing molecular biology experiments.Entities:
Keywords: Apolipoprotein L1; Cancer; Papillary thyroid carcinoma
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Year: 2016 PMID: 27157405 DOI: 10.1016/j.prp.2016.04.004
Source DB: PubMed Journal: Pathol Res Pract ISSN: 0344-0338 Impact factor: 3.250