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Acute promyelocytic leukemia is characterized by a chromosomal translocation involving the retinoic acid receptor alpha (RARA) gene on chromosome 17. [3] In 95% of cases of APL, the RARA gene on chromosome 17 is involved in a reciprocal translocation with the promyelocytic leukemia gene (PML) on chromosome 15, a translocation denoted as t(15;17)(q22;q21). [3]
[46] [47] [48] The most commonly mutated gene in all colorectal cancer is the APC gene, which produces the APC protein. [45] The APC protein prevents the accumulation of β-catenin protein. Without APC, β-catenin accumulates to high levels and translocates (moves) into the nucleus, binds to DNA, and activates the transcription of proto-oncogenes.
2660 17700 Ensembl ENSG00000138379 ENSMUSG00000026100 UniProt O14793 O08689 RefSeq (mRNA) NM_005259 NM_010834 RefSeq (protein) NP_005250 NP_034964 Location (UCSC) Chr 2: 190.06 – 190.06 Mb Chr 1: 53.1 – 53.11 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse In humans, the MSTN gene is located on the long (q) arm of chromosome 2 at position 32.2. Myostatin (also known as growth ...
A prospective study found that increased hepatocellular cancer risk is associated with higher levels of major circulating bile acids that were measured in people several years prior to tumor diagnosis. [104] In another study using a mouse model, it was found that dysregulated hepatic bile acids collaboratively promote liver carcinogenesis. [105]