Raloxifene-stimulated experimental breast cancer with the paradoxical actions of estrogen to promote or prevent tumor growth: A unifying concept in anti-hormone resistance

Autor: Balaburski, Gregor M., Dardes, Rita de Cássia de Maio [UNIFESP], Johnson, Michael, Haddad, Bassem, Zhu, Fang, Ross, Eric A., Sengupta, Surojeet, Klein-Szanto, Andres, Liu, Hong, Lee, Eun Sook, Kim, Helen, Jordan, V. Craig
Přispěvatelé: Georgetown Univ, Fox Chase Canc Ctr, Universidade Federal de São Paulo (UNIFESP), Northwestern Univ
Rok vydání: 2010
Předmět:
Zdroj: Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
ISSN: 1791-2423
1019-6439
DOI: 10.3892/ijo_00000687
Popis: Department of Defense, Center of Excellence SPORE in Breast Cancer Genuardi's Fund FCCC Lynn Sage Breast Cancer Research Foundation Weg Fund of Fox Chase Cancer Center Cancer Center Support Grant (CCSG) We have previously demonstrated that prolonged treatments with raloxifene (RAL) in vitro will result in phase II RAL resistance and RAL-induced tumor growth. Clinical interest prompted us to re-examine RAL resistance in vivo, particularly the effects of long-term treatments (a decade or more) on the evolution of RAL resistance. in this study, we have addressed the question of this being a reproducible phenomenon in wild-type estrogen receptor (ER)-positive human breast cell line MCF-7. MCF-7 cells cultured under estrogen-deprived conditions in the presence of 1 mu M RAL for more than a year develop RAL, resistance resulting in an independent cell line, MCF7-RAL. the MCF7-RAL cells grow in response to both estradiol E, and RAL. Fulvestrant (FUL) blocks RAL and E(2)-mediated growth. Transplantation of MCF7-RAL cells into athymic ovariectomized mice and treatment with physiologic doses of E(2) causes early E(2)-stimulated tumor growth. in contrast, continuous treatment of implanted animals with daily oral RAL (1.5 mg daily) causes growth of small tumors within 15 weeks. Continuous re-transplantation of the tumors growing in RAL-treated mice indicated that RAL, stimulated tumor growth. Tumors in the untreated mice did not grow. Bi-transplantation of MCF7-E(2) and MCF7-RAL tumors into the opposing mammary fat pads of the same ovariectomized animal demonstrated that MCF7-E(2) grew with E(2) stimulation and not with RAL. Conversely. MCF7-RAL tumors grew with RAL and not E(2) a characteristic of phase II resistance. Established phase II resistance of MCF7-RAL tumors was confirmed following up to 7 years of serial transplantation in RAL-treated athymic mice. the ER alpha was retained in these tumors. the cyclical nature of RAL resistance was confirmed and extended during a 2-year evolution of the resistant phases of the MCF7-RAL tumors. the MCF7-RAL tumors that initially were inhibited by E(2) grew in the presence of E(2) and subsequently grew with either RAL or E(2). RAL remained the major grow stimulus and RAL enhanced E(2)-stimulated growth. Subsequent transplantation of E(2) stimulated tumors and evaluations of the actions of RAL, demonstrated robust E(2)-stimulated growth that was blocked by RAL. These are the characteristics of the anti-estrogenic actions of RAL on E(2)-stimulated breast cancer growth with a minor component of phase I RAL resistance. Continuous transplantation of the phase I RAL-stimulated tumors for >8 months causes reversion to phase II resistance. These data and literature reports of the cyclical nature of anti-androgen/androgen responsiveness of prostate cancer growth, illustrate the generality of the evolution of anti-hormonal resistance in sex steroid-sensitive target tissues. Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA Fox Chase Canc Ctr, Philadelphia, PA 19111 USA Universidade Federal de São Paulo, Dept Gynecol, BR-04535001 São Paulo, Brazil Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Feinberg Sch Med, Chicago, IL 60611 USA Universidade Federal de São Paulo, Dept Gynecol, BR-04535001 São Paulo, Brazil Department of Defense, Center of Excellence: BC050277 SPORE in Breast Cancer: CA89018 FCCC: NIH P30 CA006927 Cancer Center Support Grant (CCSG): NIH P30 CA051008 Web of Science
Databáze: OpenAIRE
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