Premium
Tranilast inhibits hormone refractory prostate cancer cell proliferation and suppresses transforming growth factor β1‐associated osteoblastic changes
Author(s) -
Izumi Kouji,
Mizokami Atsushi,
Li You Qiang,
Narimoto Kazutaka,
Sugimoto Kazuhiro,
Kadono Yoshifumi,
Kitagawa Yasuhide,
Konaka Hiroyuki,
Koh Eitetsu,
Keller Evan T.,
Namiki Mikio
Publication year - 2009
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.20975
Subject(s) - tranilast , lncap , cancer research , stromal cell , medicine , prostate cancer , cell growth , cancer cell , endocrinology , cancer , biology , genetics
BACKGROUND Tranilast is a therapeutic agent used in treatment of allergic diseases, although it has been reported to show anti‐tumor effects on some cancer cells. To elucidate the effects of tranilast on prostate cancer, we investigated the mechanisms of its anti‐tumor effect on prostate cancer. METHODS The anti‐tumor effects and related mechanisms of tranilast were investigated both in vitro on prostate cancer cell lines and bone‐derived stromal cells, and in vivo on severe combined immunodeficient (SCID) mice. We verified its clinical effect in patients with advanced hormone refractory prostate cancer (HRPC). RESULTS Tranilast inhibited the proliferation of LNCaP, LNCaP‐SF, and PC‐3 cells in a dose‐dependent manner and growth of the tumor formed by inoculation of LNCaP‐SF in the dorsal subcutis and in the tibia of castrated SCID mice. Flow cytometry and TUNEL assay revealed induction of cell cycle arrest and apoptosis by tranilast. Tranilast increased expression of proteins involved in induction of cell cycle arrest and apoptosis. Coculture with bone‐derived stromal cells induced proliferation of LNCaP‐SF cells. Tranilast also suppressed secretion of transforming growth factor β1 (TGF‐β1) from bone‐derived stromal cells, which induced their differentiation. Moreover, tranilast inhibited TGF‐β1‐mediated differentiation of bone‐derived stromal cells and LNCaP‐SF cell migration induced by osteopontin. In the clinical investigation, PSA progression was inhibited in 4 of 16 patients with advanced HRPC. CONCLUSIONS These observations suggest that tranilast may be a useful therapeutic agent for treatment of HRPC via the direct inhibitory effect on cancer cells and suppression of TGF‐β1‐associated osteoblastic changes in bone metastasis. Prostate 69:1222–1234, 2009. © 2009 Wiley‐Liss, Inc.