Aristolochic acid I interferes with the expression of BLCAP tumor suppressor gene in human cells
-
Add time:07/28/2019 Source:sciencedirect.com
Aristolochic acid I (AAI) is a phytocompound that is linked to the progressive renal disease and development of human urothelial carcinoma. The bladder cancer-associated protein (BLCAP) gene exhibits a tumor suppressor function in various tumors, including bladder carcinoma. This study evaluated the effect of AAI on BLCAP expression and its associated mechanism in human cells. Administering AAI to human embryonic kidney cells (HEK293), human proximal tubule epithelial cells (HK-2) and urinary bladder cancer cells (HT-1376) significantly reduced the expression of BLCAP mRNA and protein. AAI also effectively suppressed the luciferase activities driven by BLCAP promoters of various lengths in HEK293 cells. AAI significantly reduced both activator protein 1 (AP-1) and nuclear factor-κB (NF-κB) activities in reporter assays, but further point mutations revealed that Ap-1 and NF-κB binding sites on the BLCAP promoter were not AAI-responsive elements. Application of the DNA methyltransferase inhibitor, 5-aza-2′-deoxycytidine (5-aza-dC), reversed the decline of BLCAP expression that had been induced by AAI. However, AAI exposure did not alter hypermethylation of the BLCAP promoter, determined by methyl-specific polymerase chain reaction (PCR) and bisulfate sequencing. Knocking down BLCAP in HEK293 cell line enhanced the potential for cellular migration, invasion, and proliferation, along with the induction of a capacity for anchorage-independent growth. In conclusion, AAI down-regulated the expression of BLCAP gene and the deficiency in BLCAP expression contributed to the malignant transformation of human cells, implying that BLCAP may have a role in mediating AAI-associated carcinogenesis.
We also recommend Trading Suppliers and Manufacturers of ARISTOLOCHIC ACID SODIUM SALT (cas 10190-99-5). Pls Click Website Link as below: cas 10190-99-5 suppliers
Prev:Protective effects of cyclic helix B peptide on aristolochic acid induced acute kidney injury
Next:Is aristolochic acid nephropathy a widespread problem in developing countries?) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Developmental nephrotoxicity of aristolochic acid in a zebrafish model07/31/2019
- Induction of cytochromes P450 1A1 and 1A2 suppresses formation of DNA adducts by carcinogenic aristolochic acid I in rats in vivo07/30/2019
- Is aristolochic acid nephropathy a widespread problem in developing countries?07/29/2019
- Protective effects of cyclic helix B peptide on aristolochic acid induced acute kidney injury07/27/2019
- Reduced rat plasma lysophosphatidylglycerol or lysophosphatidic acid level as a biomarker of aristolochic acid-induced renal and adipose dysfunctions07/26/2019
- Aristolochic acid I is a substrate of BCRP but not P-glycoprotein or MRP207/25/2019
- Oral exposure to aristolochic acid I induces gastric histological lesions with non-specific renal injury in rat07/24/2019
- Comparison of Aristolochic acid I derived DNA adduct levels in human renal toxicity models07/23/2019
-
Health and Chemical more >


