Trastuzumab Has Opposing Effects on SN-38-induced Double-strand Breaks and Cytotoxicity in HER2-positive Gastric Cancer Cells Depending on Administration Sequence.

Source

Center for Clinical Research, Hamamatsu University School of Medicine, 1-20-1, Handayama, Higashi-Ku, Hamamatsu, 431-3192, Japan. furuta@hama-med.ac.jp.

Abstract

Aim: We investigated the effects of trastuzumab, an anti-HER2 humanized monoclonal antibody, on DNA breaks induced by SN-38, a topoisomerase-1 inhibitor, in gastric cancer cell lines positive or negative for HER2 expression.

MATERIALS AND METHODS:

NCI-N87 (HER2+) and MKN74 (HER2-) cells were exposed to SN-38 in the presence or absence of trastuzumab. Trastuzumab was added either prior to or after SN-38. Effects of trastuzumab on the induction of gamma-H2AX, a marker of DNA double-strand breaks, the cytotoxicity of SN-38 and cell cycle progression were determined.

RESULTS:

When trastuzumab was administered following SN-38, it increased ?H2AX levels and cytotoxicity of SN-38 in NCI-N87 cells, but not in MKN74 cells. In contrast, pretreatment with trastuzumab reduced SN-38-induced ?H2AX expression and cytotoxicity of SN-38 in NCI-N87 cells, but not in MKN74 cells. Trastuzumab delayed cell cycle progression in NCI-N87 cells only.

CONCLUSION:

Trastuzumab has opposing effects on SN-38-induced double-strand breaks and cytotoxicity depending on the order of administration of the two agents.

Source: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&db=PubMed&cmd=Retrieve&list_uids=22213294&dopt=Abstract

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