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This study explores the role of Anti-hTERT-siRNAs in reducing tumor growth by targeting key pathways. By downregulating hTERT, EGFR, FOSL1, and LAMC2, we observed significant tumor suppression and increased apoptosis in cancer cells. The findings suggest that manipulating the hTERT pathway could be a promising therapeutic approach for enhancing cancer treatment outcomes. Further research is needed to fully understand the mechanistic implications of these targets in tumor biology.
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Anti-hTERT-siRNAs ? EGFR hTERT FOSL1 LAMC2 Tumorwachstum Apoptose