Targeted Gene Delivery Therapies for Cervical Cancer

被引:40
作者
Ayen, Angela [1 ,2 ]
Jimenez Martinez, Yaiza [3 ,4 ]
Boulaiz, Houria [2 ,3 ,4 ,5 ]
机构
[1] San Cecilio Univ Hosp, Dept Dermatol, Granada 18016, Spain
[2] Univ Granada, Dept Human Anat & Embryol, Granada 18016, Spain
[3] Univ Granada, Biopathol & Med Regenerat Inst IBIMER, Granada 18016, Spain
[4] SAS Univ Granada, Biosanitary Inst Granada Ibs GRANADA, Granada 18016, Spain
[5] Univ Granada, Excellence Res Unit Modeling Nat MNat, Granada 18016, Spain
关键词
cervical cancer; targeted gene therapy; delivery systems; immunopotentiation; cervical cancer stem cells; INTRAEPITHELIAL NEOPLASIA 2/3; HPV DNA VACCINATION; HUMAN-PAPILLOMAVIRUS; ONCOLYTIC ADENOVIRUS; CELL-GROWTH; IN-VITRO; HELA-CELLS; PROMOTES APOPTOSIS; DOWN-REGULATION; DOUBLE-BLIND;
D O I
10.3390/cancers12051301
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite being largely preventable through early vaccination and screening strategies, cervical cancer is the most common type of gynecological malignancy worldwide and constitutes one of the leading causes of cancer deaths in women. Patients with advanced or recurrent disease have a very poor prognosis; hence, novel therapeutic modalities to improve clinical outcomes in cervical malignancy are needed. In this regard, targeted gene delivery therapy is presented as a promising approach, which leads to the development of multiple strategies focused on different aspects. These range from altered gene restoration, immune system potentiation, and oncolytic virotherapy to the use of nanotechnology and the design of improved and enhanced gene delivery systems, among others. In the present manuscript, we review the current progress made in targeted gene delivery therapy for cervical cancer, the advantages and drawbacks and their clinical application. At present, multiple targeted gene delivery systems have been reported with encouraging preclinical results. However, the translation to humans has not yet shown a significant clinical benefit due principally to the lack of efficient vectors. Real efforts are being made to develop new gene delivery systems, to improve tumor targeting and to minimize toxicity in normal tissues.
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页数:33
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