2007
DOI: 10.1016/j.yexcr.2007.03.006
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High tolerance to apoptotic stimuli induced by serum depletion and ceramide in side-population cells: High expression of CD55 as a novel character for side-population

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Cited by 37 publications
(32 citation statements)
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“…This broad spectrum is also observed in MCF7 breast cancer cell line (22). Very recently, we found that CD55-high population in the MCF7 cells is resistant to apoptotic stimuli and forms colonies in vitro more efficiently than CD55-low population (22). CD55 expression level is higher in SP cells than in non-SP of MCF7 cells.…”
supporting
confidence: 59%
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“…This broad spectrum is also observed in MCF7 breast cancer cell line (22). Very recently, we found that CD55-high population in the MCF7 cells is resistant to apoptotic stimuli and forms colonies in vitro more efficiently than CD55-low population (22). CD55 expression level is higher in SP cells than in non-SP of MCF7 cells.…”
supporting
confidence: 59%
“…Staining of HT29 colon cancer cell line with anti-CD55 antibody showed a broad spectrum of expression levels among cancer cells (19). This broad spectrum is also observed in MCF7 breast cancer cell line (22). Very recently, we found that CD55-high population in the MCF7 cells is resistant to apoptotic stimuli and forms colonies in vitro more efficiently than CD55-low population (22).…”
mentioning
confidence: 60%
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“…The possible toxicity of Hoechst 33342 may create bias by selectively injuring non-SP cells thus bias any comparative tests of cancer SP and Non-SP cells. 80,81 However, recent work by Chiba et al, demonstrated that the difference of Hoechst 33342 toxicity on cancer SP and Non-SP cells is marginal and may not explain the failure of Non-SP cells to sustain proliferation in vitro or to form tumors in vivo. 42 To reduce the potential bias by Hoechst 33342, alternative low toxicity dyes, like Cycle Violet (also known as Vybrant Violet), could be used for SP staining.…”
Section: Isolation and Enrichment Of Cancer Stem Cellsmentioning
confidence: 99%
“…These rare cell populations possessed an increased ability to form tumors when they were injected into etoposide-treated NOD/ SCID mice; as few as 100 CD44 + /cd24 -human breast cancer cells could recapitulate the human mammary tumors, whereas the injection of 10,000 cells with other phenotypes failed to give rise to tumors (2). Since then, several techniques have been established to isolate or enrich for tumorigenic breast cancer stem cells (BCSCs), including side-population (SP) separation and mammosphere culture (6,7). In breast cancer, the mammosphere culture system has been widely used to identify and enrich for putative stem cells using breast cancer cell lines (8).…”
Section: Introductionmentioning
confidence: 99%