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Oncol Lett. 2017 May;13(5):3767-3773. doi: 10.3892/ol.2017.5918. Epub 2017 Mar 27.

Antitumor activity of 7-O-succinyl macrolactin A tromethamine salt in the mouse glioma model.

Oncology letters

Jun Jin, Suh Hee Choi, Jung Eun Lee, Jin-Deok Joo, Jung Ho Han, Su-Young Park, Chae-Yong Kim

Affiliations

  1. Department of Neurosurgery, Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do 13620, Republic of Korea.
  2. Department of Neurosurgery, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
  3. Research and Development Center, Daewoo Pharmaceutical Ind. Co., Ltd., Busan 49393, Republic of Korea.

PMID: 28529591 PMCID: PMC5431494 DOI: 10.3892/ol.2017.5918

Abstract

Chemoradiotherapy with temozolomide is the current standard treatment option for patients with glioblastoma. However, the majority of patients with glioblastoma survive for <2 years. Therefore, it is necessary to develop more effective therapeutic strategies for the treatment of glioblastoma. 7-O-succinyl macrolactin A tromethamine salt (SMA salt), a macrolactin compound, is known to possess an antiangiogenic activity. The present study investigated the antitumor effects of SMA salt in the treatment of glioblastoma by evaluating

Keywords: 7-O-succinyl macrolactin A tromethamine salt; glioblastoma; invasion; macrolactin A; migration

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