Prospects of Molecularly-Targeted Therapies for Cervical Cancer Treatment

被引:61
作者
de Freitas, Antonio Carlos [1 ]
Gomes Leitao, Maria da Conceicao [1 ]
Coimbra, Eliane Campos [1 ]
机构
[1] Univ Fed Pernambuco, Lab Mol Studies & Expt Therapy LEMTE, Dept Genet, Ctr Biol Sci, BR-50670901 Recife, PE, Brazil
关键词
Cervical cancer; HPV; microRNA; molecular targets; therapy; HUMAN-PAPILLOMAVIRUS TYPE-16; PHASE-II TRIAL; SQUAMOUS-CELL-CARCINOMA; CYCLOOXYGENASE-2 INHIBITOR CELECOXIB; POTENTIAL THERAPEUTIC TARGET; TUMOR-SUPPRESSIVE MIR-34A; GROWTH-FACTOR RECEPTOR; SHORT INTERFERING RNA; IN-VITRO; DNA-REPLICATION;
D O I
10.2174/1389450116666141205150942
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Cervical cancer is the third most common cancer among women worldwide and is responsible for 275.000 deaths each year. The development of cervical cancer has been linked to cell cycle disturbances caused by persistent expression of high-risk HPV oncoproteins (E5, E6 and E7), which modulate the expression of host genes and cellular microRNAs. An estimated 5 million women throughout the world are currently infected by HPV and several of them will develop invasive cervical cancer. Despite failures in conventional screening tests, approved therapies have no direct effect on HPV infection. In view of this, effective therapy for cervical cancer is still urgently needed, particularly in developing countries where more than 85% of fatal cases occur. In this paper we review the current molecular targeted therapies which are being explored and may have a significant impact on the treatment of HPV-related cervical dysplasia and carcinoma.
引用
收藏
页码:77 / 91
页数:15
相关论文
共 220 条
[1]
In vivo antitumor effect of an intracellular single- chain antibody fragment against the E7 oncoprotein of human papillomavirus 16 [J].
Accardi, Luisa ;
Paolini, Francesca ;
Mandarino, Angela ;
Percario, Zulema ;
Di Bonito, Paola ;
Di Carlo, Valentina ;
Affabris, Elisabetta ;
Giorgi, Colomba ;
Amici, Carla ;
Venuti, Aldo .
INTERNATIONAL JOURNAL OF CANCER, 2014, 134 (11) :2742-2747
[2]
Alvarez-Salas Luis M, 2007, Curr Drug Discov Technol, V4, P208, DOI 10.2174/157016307782109661
[3]
Nucleic Acids as Therapeutic Agents [J].
Alvarez-Salas, Luis M. .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2008, 8 (15) :1379-1404
[4]
[Anonymous], 2011, J NUCL ACIDS INVESTI, DOI DOI 10.4081/JNAI.2011.2583
[5]
[Anonymous], 2003, J NATL CANC I
[6]
Human papillomavirus type 16 integration in cervical carcinoma in situ and in invasive cervical cancer [J].
Arias-Pulido, Hugo ;
Peyton, Cheri L. ;
Joste, Nancy E. ;
Vargas, Hernan ;
Wheeler, Cosette M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (05) :1755-1762
[7]
Oncogenic PI3K deregulates transcription and translation [J].
Bader, AG ;
Kang, SY ;
Zhao, L ;
Vogt, PK .
NATURE REVIEWS CANCER, 2005, 5 (12) :921-929
[8]
Bader Andreas G., 2012, Frontiers in Genetics, V3, P120, DOI 10.3389/fgene.2012.00120
[9]
Translational approaches to improving cervical screening [J].
Baldwin, P ;
Laskey, R ;
Coleman, N .
NATURE REVIEWS CANCER, 2003, 3 (03) :217-226
[10]
Identification of inhibitors to papillomavirus type 16 E6 protein based on three-dimensional structures of interacting proteins [J].
Baleja, James D. ;
Cherry, Jonathan J. ;
Liu, Zhiguo ;
Gao, Hua ;
Nicklaus, Marc C. ;
Voigt, Johannes H. ;
Chen, Jason J. ;
Androphy, Elliot J. .
ANTIVIRAL RESEARCH, 2006, 72 (01) :49-59