Scientific reports · 2011
Potential role of LMP2 as tumor-suppressor defines new targets for uterine leiomyosarcoma therapy.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Hayashi Takuma, Horiuchi Akiko, Sano Kenji, Hiraoka Nobuyoshi, Kasai Mari, Ichimura Tomoyuki, Sudo Tamotsu, Tagawa Yoh-Ichi, Nishimura Ryuichiro, Ishiko Osamu, Kanai Yae, Yaegashi Nobuo, Aburatani Hiroyuki, Shiozawa Tanri, Konishi Ikuo
Аннотация
Although the majority of smooth muscle neoplasms found in the uterus are benign, uterine leiomyosarcoma (LMS) is extremely malignant, with high rates of recurrence and metastasis. We earlier reported that mice with a homozygous deficiency for LMP2, an interferon (IFN)-γ-inducible factor, spontaneously develop uterine LMS. The IFN-γ pathway is important for control of tumor growth and invasion and has been implicated in several cancers. In this study, experiments with human and mouse uterine tissues revealed a defective LMP2 expression in human uterine LMS that was traced to the IFN-γ pathway and the specific effect of JAK-1 somatic mutations on the LMP2 transcriptional activation. Furthermore, analysis of a human uterine LMS cell line clarified the biological significance of LMP2 in malignant myometrium transformation and cell cycle, thus implicating LMP2 as an anti-tumorigenic candidate. This role of LMP2 as a tumor suppressor may lead to new therapeutic targets in human uterine LMS.