Arginine deprivation induces endoplasmic reticulum stress in human solid cancer cells

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• 作者：Yaroslav Bobak^a ; ¹ ; ^{bobakyaroslav@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Yuliya Kurlishchuk^a ; ^b ; ¹ ; ^{kurlishchukyuliya@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Bozhena Vynnytska-Myronovska^a ; ^b ; ² ; ^{b.vynnytskamyronovska@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Olesia Grydzuk^a ; ^{olesia.hr@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Galyna Shuvayeva^a ; ^{galinash1977@mail.ru" class="auth_mail" title="E-mail the corresponding author} ; Maria J. Redowicz^c ; ^{jolanta@nencki.gov.pl" class="auth_mail" title="E-mail the corresponding author} ; Leoni A. Kunz-Schughart^b ; ^d ; ^{leoni.kunz-schughart@oncoray.de" class="auth_mail" title="E-mail the corresponding author} ; Oleh Stasyk^a ; ^{stasyk@cellbiol.lviv.ua" class="auth_mail" title="E-mail the corresponding author}
• 关键词：CHX ; cycloheximide ; DMSO ; dimethyl sulfoxide ; ER ; endoplasmic reticulum ; Tm ; tunicamycin ; UPR ; unfolded protein response ; XBP1s ; spliced form of XBP1
• 刊名：International Journal of Biochemistry and Cell Biology
• 出版年：2016
• 出版时间：January 2016
• 年：2016
• 卷：70
• 期：Complete
• 页码：29-38
• 全文大小：2274 K

文摘

Deprivation for the single amino acid arginine is a rapidly developing metabolic anticancer therapy, which allows growth control in a number of highly malignant tumors. Here we report that one of the responses of human solid cancer cells to arginine starvation is the induction of prolonged endoplasmic reticulum (ER) stress and activation of the unfolded protein response (UPR). Systematic study of two colorectal carcinoma HCT-116 and HT29, glioblastoma U251 MG and ovarian carcinoma SKOV3 cell lines revealed, however, that the ER stress triggered by the absence of arginine does not result in massive apoptosis despite a profound upregulation of the proapoptotic gene CHOP. Instead, Akt- and MAPK-dependent pathways were activated which may counteract proapoptotic signaling. Treatment with DMSO as a disaggregating agent or with cycloheximide to block protein synthesis reduced ER stress evoked by arginine deprivation. On the other hand, ER stress and apoptosis induction in arginine-starved cells could be critically augmented by the arginine analog of plant origin canavanine, but not by the classic ER stress inducer tunicamycin. Our data suggest that canavanine treatment applied under the lack of arginine may enhance the efficacy of arginine deprivation-based anticancer therapy.