| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2120417 | Drug Resistance Updates | 2011 | 17 Pages |
Colorectal cancer is the second leading cause of cancer-related deaths in the world. Despite many therapeutic opportunities, prognosis remains dismal for patients with metastatic disease, and a significant portion of early-stage patients develop recurrence after chemotherapy. Epigenetic gene regulation is a major mechanism of cancer initiation and progression, through the inactivation of several tumor suppressor genes. Emerging evidence indicates that epigenetics may also play a key role in the development of chemoresistance. In the present review, we summarize epigenetic mechanisms triggering resistance to three commonly used agents in colorectal cancer: 5-fluorouracil, irinotecan and oxaliplatin. Those epigenetic biomarkers may help stratify colorectal cancer patients and develop a tailored therapeutic approach. In addition, epigenetic modifications are reversible through specific drugs: histone-deacetylase and DNA-methyl-transferase inhibitors. Preclinical studies suggest that these drugs may reverse chemoresistance in colorectal tumors. In conclusion, an epigenetic approach to colorectal cancer chemoresistance may pave the way to personalized treatment and to innovative therapeutic strategies.
► Colorectal cancer (CRC) is the second cause of cancer-related deaths in the world. ► Despite therapeutic advancements, CRC drug resistance is the main cause of treatment failure. ► Epigenetics may play a key role in chemoresistance. ► Epigenetic mechanisms of resistance to 5-FU, irinotecan and oxaliplatin in CRC are described. ► Drug resistance modulation by epigenetic drugs may contribute to improve therapeutic outcome.
