scispace - formally typeset
S

Samir Satih

Researcher at French Institute of Health and Medical Research

Publications -  21
Citations -  693

Samir Satih is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Cancer & Breast cancer. The author has an hindex of 14, co-authored 21 publications receiving 654 citations. Previous affiliations of Samir Satih include University of Clermont-Ferrand.

Papers
More filters
Journal Article

Soy Phytoestrogens Modify DNA Methylation of GSTP1, RASSF1A, EPH2 and BRCA1 Promoter in Prostate Cancer Cells

TL;DR: Epigenetic modifications of DNA, such as the promoter CpG island demethylation of tumor suppressor genes, might be related to the protective effect of soy on prostate cancer.
Journal ArticleDOI

Genistein and daidzein act on a panel of genes implicated in cell cycle and angiogenesis by Polymerase Chain Reaction arrays in human prostate cancer cell lines.

TL;DR: Modulations of cyclin-dependent kinase-related pathway genes, DNA damage-signaling pathway and a down-regulation of EGF and IGF are demonstrated in men diagnosed with prostate cancer by using different prostate cancer cell lines.
Journal ArticleDOI

Gene signature of breast cancer cell lines treated with lycopene.

TL;DR: In this article, an oligonucleotide microarray approach was used to investigate the responsiveness of breast cancer genes to lycopene and to better understand the molecular mechanisms underlying the effects of Lycopene.
Journal Article

DNA repair gene ERCC2, XPC, XRCC1, XRCC3 polymorphisms and associations with bladder cancer risk in a French cohort.

TL;DR: The Gln allele of the XPC 939 polymorphism was found to be associated with an increase in bladder cancer risk, which is seen as a polygenic disease.
Journal Article

Genetic polymorphisms in CYP1A1, CYP1B1, COMT, GSTP1 and NAT2 genes and association with bladder cancer risk in a French cohort.

TL;DR: Investigation of the association between functional polymorphisms in CYP1A1, CYp1B1, COMT, GSTP1 and NAT2 genes and BC risk consistent with previous literature among Caucasian populations found no statistically significant effects on BC risk.