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Upregulation of TRAG3 gene in urothelial carcinoma of the bladder
Journal article   Open access   Peer reviewed

Upregulation of TRAG3 gene in urothelial carcinoma of the bladder

Jose A Karam, Sandra Huang, Jinhai Fan, Jennifer Stanfield, Roger A Schultz, Rey-Chen Pong, Xiankai Sun, Ralph P Mason, Xian-Jin Xie, Gang Niu, …
International journal of cancer, Vol.128(12), pp.2823-2832
06/15/2011
DOI: 10.1002/ijc.25631
PMCID: PMC3082622
PMID: 20734393
url
https://doi.org/10.1002/ijc.25631View
Published (Version of record) Open Access

Abstract

Conventional chemotherapy is commonly used for advanced stages of bladder cancer with modest success and high morbidity. Identifying markers of resistance will allow clinicians to tailor treatment to a specific patient population. T24-tumorigenic cell line was grown orthotopically in nude mice and monitored using bioluminescence imaging and microcomputed tomography until they developed metastases. Stable sublines were then developed from primary bladder (T24-P), lung (T24-L) and bone (T24-B) tissues. Chromosomal analysis and DNA microarray were used to characterize these sublines. Real-time quantitative polymerase chain reaction and immunohistochemistry were used for validation. Epigenetic modifiers were used to study gene regulation. The cell viability was quantified with MTT assay. Chromosomal analysis revealed multiple alterations in metastatic cell lines compared to T24-P. DNA microarray analysis showed that taxol resistance-associated gene (TRAG) 3 was the most upregulated gene. From real-time quantitative polymerase chain reaction and immunohistochemistry, TRAG3 was significantly higher in T24-L and T24-B than T24-P. TRAG3 gene expression is likely controlled by DNA methylation but not histone acetylation. Interestingly, T24-B and T24-L cells were more resistant than T24-P to treatment with antimicrotubule agents such as docetaxel, paclitaxel and vinblastine. TRAG3 mRNA expression was higher in 20% of patients with ≤ pT2 (n = 10) and 60% of patients with ≥ pT3 (n = 20) compared to normal adjacent tissue (p = 0.05). In addition, the median TRAG3 expression was 6.7-fold higher in ≥ pT3 tumors compared to ≤ pT2 tumors. Knowing the status of TRAG3 expression could help clinicians tailor treatment to a particular patient population that could benefit from treatment, while allocating patients with resistant tumors to new experimental therapies.
Up-Regulation Oligonucleotide Array Sequence Analysis Humans Middle Aged Male DNA Primers Neoplasm Metastasis Animals Urinary Bladder Neoplasms - genetics Carcinoma, Transitional Cell - pathology Mice, Nude Base Sequence Polymerase Chain Reaction Urinary Bladder Neoplasms - pathology Aged, 80 and over Adult Female Aged Mice Neoplasm Proteins - genetics Carcinoma, Transitional Cell - genetics

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