Department of Biochemistry, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Kidney Research Center, Department of Nephrology, Chang Gung Memorial Hospital, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
FASEB J. 2018 May;32(5):2601-2614. doi: 10.1096/fj.201700094R. Epub 2018 Jan 10.
Argininosuccinate synthetase 1 (ASS1) is a rate-limited enzyme in arginine biosynthesis. The oncogenic potential of ASS1 in terms of prognosis and cancer metastasis in arginine prototrophic gastric cancer (GC) remains unclear at present. We identify differentially expressed proteins in microdissected GC tumor cells relative to adjacent nontumor epithelia by isobaric mass tag for relative and absolute quantitation proteomics analysis. GC cells with stable expression or depletion of ASS1 were further analyzed to identify downstream molecules. We investigated their effects on chemoresistance and cell invasion in the presence or absence of arginine. ASS1 was highly expressed in GC and positively correlated with GC aggressiveness and poor outcome. Depletion of ASS1 led to inhibition of tumor growth and decreased cell invasion via induction of autophagy-lysosome machinery, resulting in degradation of active β-catenin, Snail, and Twist. Ectopic expression of ASS1 in GC cells reversed these effects and protected cancer cells from chemotherapy drug-induced apoptosis via activation of the AKT-mammalian target of rapamycin signaling pathway. ASS1 contributes to GC progression by enhancing aggressive potential resulting from active β-catenin, Snail, and Twist accumulation. Our results propose that ASS1 might contribute to GC metastasis and support its utility as a prognostic predictor of GC.-Tsai, C.-Y., Chi, H.-C., Chi, L.-M., Yang, H.-Y., Tsai, M.-M., Lee, K.-F., Huang, H.-W., Chou, L.-F., Cheng, A.-J., Yang, C.-W., Wang, C.-S., Lin, K.-H. Argininosuccinate synthetase 1 contributes to gastric cancer invasion and progression by modulating autophagy.
精氨酸琥珀酸合成酶 1(ASS1)是精氨酸生物合成中的限速酶。目前,ASS1 在精氨酸原养型胃癌(GC)中的预后和癌症转移方面的致癌潜力尚不清楚。我们通过等压质量标签相对和绝对定量蛋白质组学分析鉴定了微切割 GC 肿瘤细胞相对于相邻非肿瘤上皮的差异表达蛋白。进一步分析了稳定表达或耗尽 ASS1 的 GC 细胞,以鉴定下游分子。我们研究了它们在存在或不存在精氨酸的情况下对化学抗性和细胞侵袭的影响。ASS1 在 GC 中高表达,与 GC 的侵袭性和不良预后呈正相关。ASS1 的耗竭导致通过诱导自噬-溶酶体机制抑制肿瘤生长和降低细胞侵袭,导致活性 β-连环蛋白、Snail 和 Twist 的降解。GC 细胞中 ASS1 的异位表达逆转了这些效应,并通过激活 AKT-雷帕霉素靶蛋白信号通路保护癌细胞免受化疗药物诱导的细胞凋亡。ASS1 通过增强活性 β-连环蛋白、Snail 和 Twist 的积累来促进 GC 的侵袭和进展。我们的研究结果表明,ASS1 可能有助于 GC 转移,并支持其作为 GC 预后预测因子的用途。-蔡,C.-Y.,池,H.-C.,池,L.-M.,杨,H.-Y.,蔡,M.-M.,李,K.-F.,黄,H.-W.,周,L.-F.,程,A.-J.,杨,C.-W.,王,C.-S.,林,K.-H.。精氨酸琥珀酸合成酶 1 通过调节自噬促进胃癌侵袭和进展。