Research output: Contribution to journal › Article › peer-review
Highly cytotoxic gold(i)-phosphane dithiocarbamate complexes trigger an ER stress-dependent immune response in ovarian cancer cells. / Le, Hai Van; Babak, Maria V.; Ehsan, Muhammad Ali et al.
In: Dalton Transactions, Vol. 49, No. 22, 14.06.2020, p. 7355-7363.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Highly cytotoxic gold(i)-phosphane dithiocarbamate complexes trigger an ER stress-dependent immune response in ovarian cancer cells
AU - Le, Hai Van
AU - Babak, Maria V.
AU - Ehsan, Muhammad Ali
AU - Altaf, Muhammad
AU - Reichert, Lisa
AU - Gushchin, Artem L.
AU - Ang, Wee Han
AU - Isab, Anvarhusein A.
PY - 2020/6/14
Y1 - 2020/6/14
N2 - Ovarian cancer is a highly aggressive disease which is treated by surgery and platinum chemotherapy. However, a significant proportion of treated patients develop resistance to platinum treatment resulting in tumor relapse. Acquired platinum resistance has been recently correlated with activation of pro-survival endoplasmic reticulum (ER) stress responses. We hypothesized that Au complexes that induce severe ER stress might counteract pro-survival cellular attempts leading to the ER stress-mediated apoptosis and reduced platinum resistance. In this work, we prepared a series of highly cytotoxic AuI-dialkyldithiocarbamate complexes and investigated their anticancer potential in ovarian cancer cells. Complexes demonstrated surprisingly low stability in chloroform, resulting in the formation of an Au chain polymer, which also displayed excellent cytotoxicity. Lead complex2induced oxidative stress and ER stress-mediated p53-independent apoptosis associated with PARP cleavage and cell cycle arrest at G2/M phase. Importantly,2caused the surface exposure of calreticulin (CRT), which is the first step in the activation of cellular immunogenic response.
AB - Ovarian cancer is a highly aggressive disease which is treated by surgery and platinum chemotherapy. However, a significant proportion of treated patients develop resistance to platinum treatment resulting in tumor relapse. Acquired platinum resistance has been recently correlated with activation of pro-survival endoplasmic reticulum (ER) stress responses. We hypothesized that Au complexes that induce severe ER stress might counteract pro-survival cellular attempts leading to the ER stress-mediated apoptosis and reduced platinum resistance. In this work, we prepared a series of highly cytotoxic AuI-dialkyldithiocarbamate complexes and investigated their anticancer potential in ovarian cancer cells. Complexes demonstrated surprisingly low stability in chloroform, resulting in the formation of an Au chain polymer, which also displayed excellent cytotoxicity. Lead complex2induced oxidative stress and ER stress-mediated p53-independent apoptosis associated with PARP cleavage and cell cycle arrest at G2/M phase. Importantly,2caused the surface exposure of calreticulin (CRT), which is the first step in the activation of cellular immunogenic response.
UR - http://www.scopus.com/inward/record.url?scp=85086285658&partnerID=8YFLogxK
U2 - 10.1039/d0dt01411g
DO - 10.1039/d0dt01411g
M3 - Article
C2 - 32432621
AN - SCOPUS:85086285658
VL - 49
SP - 7355
EP - 7363
JO - Dalton Transactions
JF - Dalton Transactions
SN - 1477-9226
IS - 22
ER -
ID: 24519397