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. 2022 May 10;53:102331. doi: 10.1016/j.redox.2022.102331

Table 1.

Expression and role of CBS in various cancers.

Colorectal cancer Ovarian cancer Breast cancer Urothelial cell carcinoma of bladder Lung adeno-carcinoma Renal cancers Oral and esophageal carcinoma Extrahepatic cholangio-carcinoma Gallbladder adenocarcinoma Gastric cancer Multiple myeloma Liver cancer Glioma, glioblastoma
CBS protein expression in clinical tumor tissue relative to surrounding normal Higher Higher Higher Higher Higher Higher Higher Higher Higher Higher Not yet assessed Lower Lower
Correlation of CBS protein expression in clinical tumor specimen with disease stage Correlation confirmed both in terms of colon cancer stage and also in terms of progression from polyp formation to colon adenocarcinoma formation Correlation confirmed Correlation confirmed for basal-like cancer Not yet assessed Not yet assessed Inconclusive data Not yet assessed Correlation confirmed Not yet assessed Not yet assessed Not yet assessed Not yet assessed Not yet assessed
CBS mRNA expression in clinical tumor tissue relative to surrounding normal Higher Higher Higher Not yet assessed Higher Not yet assessed Not yet assessed Not yet assessed Not yet assessed Higher Higher Lower Lower
Correlation of CBS mRNA expression in clinical tumor tissues with clinical prognosis Higher CBS mRNA is associated with worse clinical outcomes in several (but not all) published analyses Higher CBS mRNA is associated with worse clinical outcomes Higher CBS mRNA is associated with worse clinical outcomes Higher CBS mRNA tends to be associated with better clinical outcomes. Higher CBS mRNA is associated with worse clinical outcomes. Higher CBS mRNA is associated with worse clinical outcomes (especially in renal clear cell carcinoma) Not yet assessed Higher CBS mRNA is associated with worse clinical outcomes. Not yet assessed Higher CBS mRNA is associated with worse clinical outcomes and poorer chemotherapy responses Not yet assessed Higher CBS mRNA is associated with better clinical outcomes. Higher CBS mRNA tends to be associated with better clinical outcomes.
Expression in human cancer cell lines High expression: HCT116, LoVo, HT-29, DLD-1, SW480, CTC-MCC-41 High expression: OV202, SKOV3, A2780, A2780/CP-70, CP20, OV90,
OVCAR3,
OVCAR4,
OVCAR5, OVCA429
High expression: MDA-MB-231 MDA-MB-435S, MDA-MB-468, MCF-7, Hs578T, Cal51, HCC1143 High expression: RT4, SW780, 5637, T24, EJ, UM-UC-3 High expression in A549, H522, H1944, 95D, Calu-6 Average expression: Caki-1, 786-O, 769-P is comparable to non-transformed cell controls Variable expression ranging from non-detectable to high: KYSE510, KYSE150, KYSE140, Eca109, EC9706, TE-13, KYSE70, KYSE450 Not yet assessed Not yet assessed Average expression: BGC-823, SGC-7901 Average/low expression: U266 Relatively high CBS expression: HepG2, SMMC-7721, BEL-7402, BEL-7404 Relatively low CBS expression: U87-MG, hGBM 23, hGBM 124, hGBM 3691, BT142, TS603, NCH1681
Effect of CBS silencing in human cancer cell lines in vitro Inhibition of tumor growth, potentiation of the effect of chemotherapy Inhibition of tumor growth, potentiation of the effect of chemotherapy Inhibition of tumor growth, potentiation of the effect of immune cell mediated tumor killing Not yet assessed Inhibition of tumor growth, potentiation of the effect of chemotherapy Not yet assessed Inhibition of tumor growth Not yet assessed Not yet assessed Not yet assessed Not yet assessed Variable effects: either pro- or antiproliferative and either cytotoxic or cytoprotective actions in various hepatoma cell lines Stimulation of tumor growth
Effect of CBS silencing in human cancer cell lines on tumor growth in tumor-bearing mice Inhibition of tumor growth Inhibition of tumor growth, potentiation of the effect of chemotherapy Not yet assessed Not yet assessed Not yet assessed Not yet assessed Not yet assessed Not yet assessed Not yet assessed Not yet assessed Not yet assessed Enhancement of tumor growth Enhancement of tumor growth