Bentamapimod (JNK Inhibitor AS602801) Induces Regression of Endometriotic Lesions in Animal Models

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Bentamapimod, a JNK inhibitor, reduced endometriotic lesion size in rodent models by 29-48% and suppressed inflammatory cytokines while enhancing natural killer cell activity.

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This study evaluated the c-Jun N-terminal kinase inhibitor bentamapimod (AS602801) in two rodent endometriosis models, including nude mice bearing xenografts from women with endometriosis (BWE) and an autologous rat model, and also tested its effects in human endometrial organ cultures. In nude mice, AS602801 monotherapy produced 29% regression of BWE lesions, while medroxyprogesterone acetate or progesterone alone did not, and AS602801 combined with MPA increased regression to 38%; in the autologous rat model, AS602801 induced 48% regression versus 84% for a GnRH antagonist, with AS602801 lowering inflammatory cytokines in lesions and increasing natural killer cell activity without apparent negative effects on the uterus. In human organ cultures, AS602801 reduced MMP-3 release, whereas PR/MPA failed to suppress MMP-3 in BWE-derived cultures, but AS602801 alone or with MPA did, and the authors state this indicates JNK inhibition can overcome progesterone resistance. This paper is centrally about endometriosis — it tests bentamapimod/JNK inhibition for regression of endometriotic lesions and suppression of cytokines and MMP-3 in animal models and human organ culture models of the disease.

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Abstract

Endometriosis is an estrogen (ER)-dependent gynecological disease caused by the growth of endometrial tissue at extrauterine sites. Current endocrine therapies address the estrogenic aspect of disease and offer some relief from pain but are associated with significant side effects. Immune dysfunction is also widely believed to be an underlying contributor to the pathogenesis of this disease. This study evaluated an inhibitor of c-Jun N-terminal kinase, bentamapimod (AS602801), which interrupts immune pathways, in 2 rodent endometriosis models. Treatment of nude mice bearing xenografts biopsied from women with endometriosis (BWE) with 30 mg/kg AS602801 caused 29% regression of lesion. Medroxyprogesterone acetate (MPA) or progesterone (PR) alone did not cause regression of BWE lesions, but combining 10 mg/kg AS602801 with MPA caused 38% lesion regression. In human endometrial organ cultures (from healthy women), treatment with AS602801 or MPA reduced matrix metalloproteinase-3 (MMP-3) release into culture medium. In organ cultures established with BWE, PR or MPA failed to inhibit MMP-3 secretion, whereas AS602801 alone or MPA + AS602801 suppressed MMP-3 production. In an autologous rat endometriosis model, AS602801 caused 48% regression of lesions compared to GnRH antagonist Antide (84%). AS602801 reduced inflammatory cytokines in endometriotic lesions, while levels of cytokines in ipsilateral horns were unaffected. Furthermore, AS602801 enhanced natural killer cell activity, without apparent negative effects on uterus. These results indicate that bentamapimod induced regression of endometriotic lesions in endometriosis rodent animal models without suppressing ER action. c-Jun N-terminal kinase inhibition mediated a comprehensive reduction in cytokine secretion and moreover was able to overcome PR resistance. Similar content being viewed by others

References

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Author information Authors and Affiliations Corresponding author Rights and permissions About this article Cite this article Palmer, S.S., Altan, M., Denis, D. et al. Bentamapimod (JNK Inhibitor AS602801) Induces Regression of Endometriotic Lesions in Animal Models. Reprod. Sci. 23, 11–23 (2016). https://doi.org/10.1177/1933719115600553 Published: Issue date: DOI: https://doi.org/10.1177/1933719115600553

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Benzothiazoles Endometriosis Endometrium Enzyme Inhibitors JNK Mitogen-Activated Protein Kinases Pyrimidines Adult Animals Benzothiazoles Benzothiazoles Cytokines Cytokines Disease Models, Animal Endometriosis Endometriosis Endometrium Endometrium Enzyme Inhibitors Enzyme Inhibitors Female

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