American Association for Cancer Research
00085472can172367-sup-187251_2_supp_4465729_p1bh90.pdf (86.75 kB)

Supplementary Figure 3 from Radioresistant Cervical Cancers Are Sensitive to Inhibition of Glycolysis and Redox Metabolism

Download (86.75 kB)
journal contribution
posted on 2023-03-31, 01:23 authored by Ramachandran Rashmi, Xiaojing Huang, John M. Floberg, Adnan E. Elhammali, Michael L. McCormick, Gary J. Patti, Douglas R. Spitz, Julie K. Schwarz

Effect of catalase over expression in the clonogenic survival of 2-DG, BSO and AUR treated cells. (A-B) Cells were seeded and transduced with Ad CAT and Ad empty viruses and CFA was done as described in the materials and methods section. (C) CaSki cells were treated with 20mM 2-DG, 1mM BSO and 100nM AUR for 24h along with or without CQ (60μM) and cell viability was determined by Alamar Blue. Statistical Analysis: (A) *p < 0.05 Ad-empty vs Ad-CAT BSO (B) p < 0.07 Ad-empty vs Ad-CAT for DG, BSO and BA. (C) ***DBA vs DBA+CQ, p<0.05, N=3.



American Society for Radiation Oncology




Highly glycolytic cervical cancers largely resist treatment by cisplatin and coadministered pelvic irradiation as the present standard of care. In this study, we investigated the effects of inhibiting glycolysis and thiol redox metabolism to evaluate them as alternate treatment strategies in these cancers. In a panel of multiple cervical cancer cell lines, we evaluated sensitivity to inhibition of glycolysis (2-deoxyglucose, 2-DG) with or without simultaneous inhibition of glutathione and thioredoxin metabolism (BSO/AUR). Intracellular levels of total and oxidized glutathione, thioredoxin reductase activity, and indirect measures of intracellular reactive oxygen species were compared before and after treatment. Highly radioresistant cells were the most sensitive to 2-DG, whereas intermediate radioresistant cells were sensitive to 2-DG plus BSO/AUR. In response to 2-DG/BSO/AUR treatment, we observed increased levels of intracellular oxidized glutathione, redox-sensitive dye oxidation, and decreased glucose utilization via multiple metabolic pathways including the tricarboxylic acid cycle. 2-DG/BSO/AUR treatment delayed the growth of tumors composed of intermediate radioresistant cells and effectively radiosensitized these tumors at clinically relevant radiation doses both in vitro and in vivo. Overall, our results support inhibition of glycolysis and intracellular redox metabolism as an effective alternative drug strategy for the treatment of highly glycolytic and radioresistant cervical cancers.Significance: This study suggests a simple metabolic approach to strike at an apparent Achilles' heel in highly glycolytic, radioresistant forms of cervical cancers, possibly with broader applications in cancer therapy. Cancer Res; 78(6); 1392–403. ©2018 AACR.