1. Alterations to the protein profile of bladder carcinoma cell lines induced by plant extract MINA-05 in vitro
- Author
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Carlos E Martucci, Melissa L. Thomas, Melanie Y. White, Tzong-Tyng Hung, Pamela J. Russell, Shiu-Fu Pang, Sharon C W Luk, Terry Nguyen-Khuong, Shona Seeto, Anna M Fitzgerald, and Bradley J. Walsh
- Subjects
Cell ,Biology ,Protein degradation ,Proteomics ,Biochemistry ,Cell Line, Tumor ,medicine ,Yucca ,Humans ,Electrophoresis, Gel, Two-Dimensional ,Molecular Biology ,Cell Proliferation ,Schisandra ,Bladder cancer ,Gene Expression Profiling ,Cancer ,Anatomy ,medicine.disease ,Molecular biology ,Neoplasm Proteins ,Gene Expression Regulation, Neoplastic ,Transitional cell carcinoma ,medicine.anatomical_structure ,Urinary Bladder Neoplasms ,Cell culture ,Phosphopyruvate Hydratase ,Cancer cell ,Soybeans ,Drugs, Chinese Herbal - Abstract
Bladder cancer (BLCa) is a severe urological cancer of both men and women that commonly recurs and once invasive, is difficult to treat. MINA-05 (CK Life Sciences Int'l, Hong Kong) is a derivative of complex botanical extracts, shown to reduce cellular proliferation of bladder and prostate carcinomas. We tested the effects of MINA-05 against human BLCa cell sublines, B8, B8-RSP-GCK, B8-RSP-LN and C3, from a transitional cell carcinoma, grade IV, to determine the molecular targets of treatment by observing the cellular protein profile. Cells were acclimatised for 48 h then treated for 72 h with concentrations of MINA-05 reflecting 1/2 IC(50), IC(50) and 2 x IC(50) (n = 3) or with vehicle, (0.5% DMSO). Dose-dependant changes in protein abundance were detected and characterised using 2-dimensional electrophoresis and MS. We identified 10 proteins that underwent changes in abundance, pI and/or molecular mass in response to treatment. MINA-05 was shown to influence proteins across numerous functional classes including cytoskeletal proteins, energy metabolism proteins, protein degradation proteins and tumour suppressors, suggesting a global impact on these cell lines. This study implies that the ability of MINA-05 to retard cellular proliferation is attributed to its ability to alter cell cycling, metabolism, protein degradation and the cancer cell environment.
- Published
- 2009