Antibody Against N-terminal Domain of Phospholipid Scramblase 1 Induces Apoptosis in Colorectal Cancer Cells Through the Intrinsic Apoptotic Pathway
Phospholipid scramblase 1 involve in biological processes including phospholipid movement, proliferation, and apoptosis. Treatment with an antiphospholipid scramblase 1 antibody (NP1) has been demonstrated to inhibit cell proliferation in colorectal cancer. This study aimed to explore the role of NP...
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Published in | Chemical biology & drug design Vol. 84; no. 1; pp. 36 - 43 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.07.2014
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Subjects | |
Online Access | Get full text |
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Summary: | Phospholipid scramblase 1 involve in biological processes including phospholipid movement, proliferation, and apoptosis. Treatment with an antiphospholipid scramblase 1 antibody (NP1) has been demonstrated to inhibit cell proliferation in colorectal cancer. This study aimed to explore the role of NP1 treatment in the apoptosis of colorectal cancer cells. Results showed that NP1 treatment significantly increases the apoptosis of colorectal cancer cells via the activation of caspase 8, caspase 9, and caspase 3. Moreover, pretreatment with a caspase 8 inhibitor did not fully prevent the apoptotic effects of NP1. Taken together, these data indicate NP1 induces cell apoptosis primary through the intrinsic apoptotic pathway. NP1 may serve as a potential therapeutic agent.
Treatment with an antiphospholipid scramblase 1 antibody (NP1) inhibited cell proliferation in colorectal cancer cell line. NP1 induced cell apoptosis primary through the intrinsic apoptotic pathway. |
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Bibliography: | Chang Gung University - No. CMRPD1A0361 and CMRPD1A0362 National Science Council of Taiwan - No. NSC 101-2321-B-182-002 ArticleID:CBDD12347 istex:E7371D0E70E4ECC8AC4ABAE34028C0E68D299D16 ark:/67375/WNG-83H9GD07-F Chang Gung Memorial Hospital ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1747-0277 1747-0285 |
DOI: | 10.1111/cbdd.12347 |