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. 2020 Jun 3;9(6):1392. doi: 10.3390/cells9061392

Table 1.

Genes/Transcription factors/Proteins associated with signalling pathway mediated drug resistance in cancer stem cells in colon carcinoma.

Genes/Transcription Factors/Proteins Functions Signalling Pathways Reference
ABCG2 A Wnt/β-catenin pathway mediated regulation of ABCG2 by miR-199a/b contributes to cisplatin resistance in colon carcinoma Wnt/β-catenin [14]
LGR5 Promotes Wnt signalling through the neutralisation of two transmembrane E3 ligases, RNF43 and ZNRF3. These enzymes remove Wnt receptors from the cell surface, thus negatively regulate Wnt signalling Wnt/β-catenin [29]
CD44, CD24, CD133, and EpCAM Expression of these markers are important in Wnt mediated CSCs growth and therapy resistance in colon carcinoma Wnt/β-catenin [30,31,32,33]
APC Restoration of mutated APC in colon carcinoma results in rapid and widespread tumour-cell differentiation and maintained inhibition without relapse of carcinoma Wnt/β-catenin [34]
β-catenin Regulates the transcription of downstream target genes to increase stem cell characteristics and subsequently therapy resistance in colon carcinoma Wnt/β-catenin [34]
Wnts Aberrant expression of Wnt proteins results in hyper activation of Wnt/β-catenin and consequently propagates stem cell characteristics Wnt/β-catenin [34]
Notch1 Higher expression of Notch 1 increases CSCs phenotype and as a result positively regulates the number of colon cancer cells resistant to therapy Notch [17]
Hes 1 Induction of Hes 1 protects cancer stem cells from differentiation Notch [17]
GLI-1 Promotes Hh mediated stem cell characteristics of colon carcinoma cells and subsequently increases therapy resistance of colon carcinoma Hedgehog [39]
Yes-associated protein 1 (YAP1) High expression of YAP target genes in the tumour was coupled increased therapy resistance of colon carcinoma and poor survival of patients Hippo [40]
YES1 YES1 regulates drug resistance of colon carcinoma through regulation of YAP1 expression Hippo [41]
MACC1 Promotes sphere formation, and increases the expression levels of pluripotent markers: CD44, CD133 and Nanog PI3K/AKT [45]