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DOI 10.1016/j.bbrc.2021.07.033

Медицинская библиотека · Biochemical and biophysical research communications · 2021

Eribulin induces tumor vascular remodeling through intussusceptive angiogenesis in a sarcoma xenograft model.

Taguchi Eiko, Horiuchi Keisuke, Senoo Akira, Susa Michiro, Inoue Masahiro, Ishizaka Takahiro, Rikitake Hajime, Matsuhashi Yusuke, Chiba Kazuhiro

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Eribulin is a novel microtubule inhibitor that, similar to other types of microtubule inhibitors, induces apoptosis by inhibiting the mitotic division of cells. Besides this direct effect on tumor cells, previous studies have shown that eribulin has the potential to induce tumor vascular remodeling in several different cancers; however, the mechanisms underlying this phenomenon remain unclear. In the present study, we aimed to elucidate whether eribulin is effective against synovial sarcoma, a relatively rare sarcoma that often affects adolescents and young adults, and to histologically investigate the microstructure of tumor vessels after the administration of eribulin. We found that eribulin exhibits potent antitumor activity against synovial sarcoma in a tumor xenograft model and that tumor vessels frequently have intervascular pillars, a hallmark of intussusceptive angiogenesis (IA), after the administration of eribulin. IA is a distinct form of angiogenesis that is involved in normal developmental processes as well as pathological conditions. Our data indicate that IA is potentially involved in eribulin-induced vascular remodeling and thereby suggest previously unacknowledged role of IA in regulating the tumor vasculature after eribulin administration.

Для цитирования: Taguchi Eiko, Horiuchi Keisuke, Senoo Akira, Susa Michiro, Inoue Masahiro, Ishizaka Takahiro, Rikitake Hajime, Matsuhashi Yusuke, Chiba Kazuhiro. Eribulin induces tumor vascular remodeling through intussusceptive angiogenesis in a sarcoma xenograft model.. Biochemical and biophysical research communications. 2021. DOI: 10.1016/j.bbrc.2021.07.033.

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