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Article Publish Status: FREE
Abstract Title:

Combination of AG490, a Jak2 inhibitor, and methylsulfonylmethane synergistically suppresses bladder tumor growth via the Jak2/STAT3 pathway.

Abstract Source:

Int J Oncol. 2014 Mar ;44(3):883-95. Epub 2014 Jan 8. PMID: 24402583

Abstract Author(s):

Youn Hee Joung, Yoon Mi Na, Young Bum Yoo, Pramod Darvin, Nipin Sp, Dong Young Kang, Sang Yoon Kim, Hong Sup Kim, Yoon Hee Choi, Hak Kyo Lee, Kyung Do Park, Byung Wook Cho, Heui Soo Kim, Jong Hwan Park, Young Mok Yang

Article Affiliation:

Youn Hee Joung

Abstract:

Human urinary bladder cancer is the fifth most common cancer, with a worldwide estimate of about two million patients. Recurrence after complete transurethral prostatic resection is the most important problem in therapy. Combination therapy is a new approach in the treatment of cancers that do not respond to current therapies. These therapies have many advantages over conventional therapies, such as fewer side-effects and greater efficiency. Research efforts using natural compounds for the elimination or growth suppression of the cancer arise from studies on methylsulfonylmethane (MSM). MSM is a natural sulfur compound with no side-effects. AG490 is a tyrosine kinase inhibitor that has been extensively used for inhibiting Jak2 in vitro and in vivo. In our study, the combinatorial effect of these two agents on human bladder cancer cell lines and xenografts was analyzed. We observed that the combination of AG490 and MSM inhibited cancer cell viability and cell migration in vitro. This combination inhibited VEGF mRNA expression in bladder cancer cell lines. In vivo experiments showed that oral administration of AG490 and MSM combination significantly inhibited the growth of tumor xenografts in mice. Our study clearly demonstrates that the predominant effect of this combination is the reduction of signaling moleculesincluding STAT3, STAT5b, IGF-1R, VEGF and VEGF-R2 which are involved in the growth, progression and metastasis of human bladder cancer. The anti-metastatic ability of this drug combination is confirmed using metastatic animal models. Therefore, this combination could have the effect of genesistasisand powerful anticancer effects against bladder cancer.

Study Type : In Vitro Study

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