Loss of ferrochelatase is protective against colon cancer cells: ferrochelatase a possible regulator of the long noncoding RNA H19
Author(s) -
Rémi Safi,
Tala MohsenKanson,
Georges Nemer,
Batoul Dekmak,
Nelly Rubeiz,
Marwan El Sabban,
Dany Nassar,
Assaad A. Eid,
Ossama Abbas,
AbdulGhani Kibbi,
Mazen Kurban
Publication year - 2019
Publication title -
journal of gastrointestinal oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.084
H-Index - 39
eISSN - 2219-679X
pISSN - 2078-6891
DOI - 10.21037/jgo.2019.03.09
Subject(s) - ferrochelatase , carcinogenesis , cancer research , colorectal cancer , downregulation and upregulation , cancer , gene knockdown , cancer cell , gene silencing , biology , medicine , cell culture , gene , heme , enzyme , genetics , biochemistry
Ferrochelatase (FECH) is the last enzyme of the heme biosynthesis pathway. Deficiency in FECH was associated with many diseases, including protoporphyria. Correlation studies showed that variations of FECH expression was detected in human carcinomas and more specifically in colon cancer. Nevertheless, the potential role of FECH in colon cancer carcinogenesis in vitro was not depicted yet.
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