Current Understanding of Epigenetics Driven Therapeutic Strategies in Colorectal Cancer Management

被引:9
作者
Deka, Dikshita [1 ]
Scarpa, Marco [2 ]
Das, Alakesh [1 ]
Pathak, Surajit [1 ]
Banerjee, Antara [1 ]
机构
[1] Chettinad Hosp & Res Inst CHRI, Chettinad Acad Res & Educ CARE, Fac Allied Hlth Sci, Dept Med Biotechnol, Chennai, Tamil Nadu, India
[2] Univ Padua, Gen Surg Unit, Azienda Osped Padova, I-35128 Padua, Italy
关键词
Colorectal cancer; inflammation; epigenetic modifications; microRNA; chromatin remodeling; colon cancer stem cells; COLON-CANCER; NONNEOPLASTIC MUCOSA; PROMOTER REGION; HISTONE H4; EXPRESSION; REPAIR; METHYLATION; PROGNOSIS; RISK; ACETYLATION;
D O I
10.2174/1871530321666210219155544
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Colorectal cancer is known to be the paramount reason for cancer deaths around the globe. It occurs due to the aggregation of epigenetic and genetic alterations in colon epithelial cells that transmute them into adenocarcinomas. Epigenetic mechanisms are interpreted as the changes in expression of the gene which is not associated with the alterations in the principal DNA sequence, while genetic changes involve modifications in oncogenes and tumor suppressor genes. The changes in the epigenetic in colon cancer that transmute colonic epithelial cells include chromatin modifications, microRNA expression, telomere length, and DNA methylation. DNA hypermethylation causes down-regulation and unsuitable expression of specific microRNA which can behave like tumor suppressor genes. Histone modifications can also influence the chromatin remodeling and gene expression, hence performs an eminent function in the silencing of the gene in colon cancer. Moreover, the telomere/telomerase interaction is a prime mechanism to embrace both cellular replicative potential and genomic instability and its malfunction plays a primary role in colon cancer. Deducing the genesis and the function of epigenetic abnormality in colon cancer pathogenesis will lead to potent prevention and therapeutic approach for colon cancer patients. Epigenetic drugs which emphasize the convertible essence of the epigenetic occurrences have accompanied the probability of epigenetic approach as a treatment alternative in colon cancer. Hence, this review is undertaken to critically envelop the recently advanced events in colorectal cancer therapies with a special emphasis on remedies targeting epigenetic modulators and future challenges towards therapeutic interventions.
引用
收藏
页码:1882 / 1894
页数:13
相关论文
共 66 条
[1]   MicroRNA-143 and-145 in colon cancer [J].
Akao, Yukihiro ;
Nakagawa, Yoshihito ;
Naoe, Tomoki .
DNA AND CELL BIOLOGY, 2007, 26 (05) :311-320
[2]   Global Histone H4 Acetylation and HDAC2 Expression in Colon Adenoma and Carcinoma [J].
Ashktorab, Hassan ;
Belgrave, Kevin ;
Hosseinkhah, Fatemeh ;
Brim, Hassan ;
Nouraie, Mehdi ;
Takkikto, Mikiko ;
Hewitt, Steve ;
Lee, Edward L. ;
Dashwood, R. H. ;
Smoot, Duane .
DIGESTIVE DISEASES AND SCIENCES, 2009, 54 (10) :2109-2117
[3]  
Banerjee A., 2019, ROLE TUMOR SPECIFIC
[4]  
Banerjee Antara, 2020, J Basic Clin Physiol Pharmacol, V31, DOI 10.1515/jbcpp-2019-0193
[5]   Strategies for targeted drug delivery in treatment of colon cancer: current trends and future perspectives [J].
Banerjee, Antara ;
Pathak, Surajit ;
Subramanium, Vimala Devi ;
Dharanivasan, G. ;
Murugesan, Ramachandran ;
Verma, Rama S. .
DRUG DISCOVERY TODAY, 2017, 22 (08) :1224-1232
[6]   Glioma stem cells promote radioresistance by preferential activation of the DNA damage response [J].
Bao, Shideng ;
Wu, Qiulian ;
McLendon, Roger E. ;
Hao, Yueling ;
Shi, Qing ;
Hjelmeland, Anita B. ;
Dewhirst, Mark W. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
NATURE, 2006, 444 (7120) :756-760
[7]   Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers [J].
Barber, Thomas D. ;
McManus, Kirk ;
Yuen, Karen W. Y. ;
Reis, Marcelo ;
Parmigiani, Giovanni ;
Shen, Dong ;
Barrett, Irene ;
Nouhi, Yasaman ;
Spencer, Forrest ;
Markowitz, Sanford ;
Velculescu, Victor E. ;
Kinzler, Kenneth W. ;
Vogelstein, Bert ;
Lengauer, Christoph ;
Hieter, Philip .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (09) :3443-3448
[8]   Telomeric recombination in mismatch repair deficient human colon cancer cells after telomerase inhibition [J].
Bechter, OE ;
Zou, Y ;
Walker, W ;
Wright, WE ;
Shay, JW .
CANCER RESEARCH, 2004, 64 (10) :3444-3451
[9]   Peutz-Jeghers syndrome: a systematic review and recommendations for management [J].
Beggs, A. D. ;
Latchford, A. R. ;
Vasen, H. F. A. ;
Moslein, G. ;
Alonso, A. ;
Aretz, S. ;
Bertario, L. ;
Blanco, I. ;
Bulow, S. ;
Burn, J. ;
Capella, G. ;
Colas, C. ;
Friedl, W. ;
Moller, P. ;
Hes, F. J. ;
Jarvinen, H. ;
Mecklin, J-P ;
Nagengast, F. M. ;
Parc, Y. ;
Phillips, R. K. S. ;
Hyer, W. ;
de Leon, M. Ponz ;
Renkonen-Sinisalo, L. ;
Sampson, J. R. ;
Stormorken, A. ;
Tejpar, S. ;
Thomas, H. J. W. ;
Wijnen, J. T. ;
Clark, S. K. ;
Hodgson, S. V. .
GUT, 2010, 59 (07) :975-986
[10]   Nuclear expression of histone deacetylases and their histone modifications predicts clinical outcome in colorectal cancer [J].
Benard, Anne ;
Goossens-Beumer, Ines J. ;
van Hoesel, Anneke Q. ;
Horati, Hamed ;
de Graaf, Wouter ;
Putter, Hein ;
Zeestraten, Eliane C. M. ;
Liefers, Gerrit-Jan ;
van de Velde, Cornelis J. H. ;
Kuppen, Peter J. K. .
HISTOPATHOLOGY, 2015, 66 (02) :270-282