Mechanism Study Of Apoptosis Induced By Microcystis Phycocyanin-mediated Photodynamic Therapy In Liver Cancer | | Posted on:2012-11-12 | Degree:Master | Type:Thesis | | Country:China | Candidate:C Y Wang | Full Text:PDF | | GTID:2214330338470848 | Subject:Cell biology | | Abstract/Summary: | PDF Full Text Request | | Phycocyanin (PC) is the major light harvesting biliprotein from Spirulina platensis etc. It is composed of two subunits—αandβsubunit, and normally exist with (αβ)3 hexamer and (αβ) 6 hexamer at room temperature. It is a water soluble, non-toxic fluorescent protein pigment with potent anti-inflammatory, anti-oxidant and even anticancer properties.Phycocyanin-mediated photodynamic therapy (PDT) was mostly used to anti-cancer study. And photosensitizer phycocyanin was usually purified from Spirulina platensis etc. This study was to explore the possibility of which phycocyanin eliminated microcystin was obtained from Microcystis (MC-PC), and to investigate possible mechanism associated with the apoptosis induced by Microcystis phycocyanin-mediated PDT (MC-PC-PDT) in HepG2 liver cancer cells. The result manifested MC-PC-PDT could inhibit HepG2 proliferation effectively at the concentration not less than 25μg/mL and cause HepG2 cells apoptosis visibly. In addition, the treatment could result in ROS accumulation which was increased greatly under the condition of 200μg/mL MC-PC for 16 h. MC-PC at 200μg/mL had the most obvious effect on mitochondrial transmembrane potential (△Ψm) collapse. Cell cycle G2/M arrest was observed after the same treatment. Blocking ROS accumulation with ROS scavengers partially suppressed△Ψm loss and cell cycle G2/M arrest, indicating that ROS accumulation play a crucial role in apoptosis induced by MC-PC-PDT. Facilitating ROS generation and finally leading to mitochondria damage, meanwhile arresting G2/M phase may be the apoptosis mechanism of MC-PC-PDT. | | Keywords/Search Tags: | Microcystis phycocyanin, PDT, Apoptosis, ROS, Mitochondrial transmembrane potential, Cell cycle | PDF Full Text Request | Related items |
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