Nucleic acid vaccination strategies for ovarian cancer

被引:5
作者
Saha, Chayanika [1 ]
Bojdo, James [1 ]
Dunne, Nicholas J. [2 ,3 ,4 ,5 ,6 ,7 ,8 ,9 ]
Duary, Raj Kumar [10 ]
Buckley, Niamh [1 ]
McCarthy, Helen O. [1 ]
机构
[1] Queens Univ Belfast, Sch Pharm, Belfast, North Ireland
[2] Dublin City Univ, Sch Mech & Mfg Engn, Dublin, Ireland
[3] Dublin City Univ, Ctr Med Engn Res, Sch Mech & Mfg Engn, Dublin, Ireland
[4] Trinity Coll Dublin, Sch Engn, Dept Mech & Mfg Engn, Dublin, Ireland
[5] Dublin City Univ, Adv Mfg Res Ctr I Form, Sch Mech & Mfg Engn, Dublin, Ireland
[6] Royal Coll Surgeons Ireland, Adv Mat & Bioengn Res Ctr AMBER, Dublin, Ireland
[7] Trinity Coll Dublin, Dublin, Ireland
[8] Dublin City Univ, Adv Proc Technol Res Ctr, Dublin, Ireland
[9] Trinity Coll Dublin, Trinity Biomed Sci Inst, Trinity Ctr Biomed Engn, Dublin, Ireland
[10] Tezpur Univ, Dept Food Engn & Technol, Tezpur, India
关键词
ovarian cancer; high grade serous carcinoma; tumour antigens; nucleic acid vaccines; DNA; mRNA; PATTERN-RECOGNITION RECEPTORS; MESSENGER-RNA EXPRESSION; CD8(+) T-CELLS; DNA VACCINATION; TESTIS ANTIGEN; TUMOR-ANTIGEN; BREAST-CANCER; PROTEIN EXPRESSION; METASTATIC BREAST; PEPTIDE VACCINES;
D O I
10.3389/fbioe.2022.953887
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
High grade serous carcinoma (HGSC) is one of the most lethal ovarian cancers that is characterised by asymptomatic tumour growth, insufficient knowledge of malignant cell origin and sub-optimal detection. HGSC has been recently shown to originate in the fallopian tube and not in the ovaries. Conventional treatments such as chemotherapy and surgery depend upon the stage of the disease and have resulted in higher rates of relapse. Hence, there is a need for alternative treatments. Differential antigen expression levels have been utilised for early detection of the cancer and could be employed in vaccination strategies using nucleic acids. In this review the different vaccination strategies in Ovarian cancer are discussed and reviewed. Nucleic acid vaccination strategies have been proven to produce a higher CD8(+) CTL response alongside CD4(+) T-cell response when compared to other vaccination strategies and thus provide a good arena for antitumour immune therapy. DNA and mRNA need to be delivered into the intracellular matrix. To overcome ineffective naked delivery of the nucleic acid cargo, a suitable delivery system is required. This review also considers the suitability of cell penetrating peptides as a tool for nucleic acid vaccine delivery in ovarian cancer.
引用
收藏
页数:22
相关论文
共 138 条
[1]   The novel cancer-testis antigen A-kinase anchor protein 4 (AKAP4) is a potential target for immunotherapy of ovarian serous carcinoma [J].
Agarwal, Sumit ;
Saini, Shikha ;
Parashar, Deepak ;
Verma, Archana ;
Sinha, Abhilasha ;
Jagadish, Nirmala ;
Batra, Aruna ;
Suri, Sushma ;
Gupta, Anju ;
Ansari, Abdul S. ;
Lohiya, Nirmal Kumar ;
Suri, Anil .
ONCOIMMUNOLOGY, 2013, 2 (05)
[2]   Ovarian Cancer, Cancer Stem Cells and Current Treatment Strategies: A Potential Role of Magmas in the Current Treatment Methods [J].
Ahmed, Nuzhat ;
Kadife, Elif ;
Raza, Ali ;
Short, Mary ;
Jubinsky, Paul T. ;
Kannourakis, George .
CELLS, 2020, 9 (03)
[3]   Pathogen recognition and innate immunity [J].
Akira, S ;
Uematsu, S ;
Takeuchi, O .
CELL, 2006, 124 (04) :783-801
[4]   Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history:: A combined analysis of 22 studies [J].
Antoniou, A ;
Pharoah, PDP ;
Narod, S ;
Risch, HA ;
Eyfjord, JE ;
Hopper, JL ;
Loman, N ;
Olsson, H ;
Johannsson, O ;
Borg, Å ;
Pasini, B ;
Radice, P ;
Manoukian, S ;
Eccles, DM ;
Tang, N ;
Olah, E ;
Anton-Culver, H ;
Warner, E ;
Lubinski, J ;
Gronwald, J ;
Gorski, B ;
Tulinius, H ;
Thorlacius, S ;
Eerola, H ;
Nevanlinna, H ;
Syrjäkoski, K ;
Kallioniemi, OP ;
Thompson, D ;
Evans, C ;
Peto, J ;
Lalloo, F ;
Evans, DG ;
Easton, DF .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (05) :1117-1130
[5]   Expression of the POTE gene family in human ovarian cancer [J].
Barger, Carter J. ;
Zhang, Wa ;
Sharma, Ashok ;
Chee, Linda ;
James, Smitha R. ;
Kufel, Christina N. ;
Miller, Austin ;
Meza, Jane ;
Drapkin, Ronny ;
Odunsi, Kunle ;
Klinkebiel, David ;
Karpf, Adam R. .
SCIENTIFIC REPORTS, 2018, 8
[6]   Efficient lysis of epithelial ovarian cancer cells by MAGE-A3-induced cytotoxic T lymphocytes using rAAV-6 capsid mutant vector [J].
Batchu, Ramesh B. ;
Gruzdyn, Oksana V. ;
Moreno-Bost, AMberly M. ;
Szmania, Susann ;
Jayandharan, Giridhararao ;
Srivastava, Arun ;
Kolli, Bala K. ;
Weaver, Donald W. ;
van Rhee, Frits ;
Gruber, Scott A. .
VACCINE, 2014, 32 (08) :938-943
[7]   Defining the molecular evolution of extrauterine high grade serous carcinoma [J].
Beirne, James P. ;
McArt, Darragh G. ;
Roddy, Aideen ;
McDermott, Clara ;
Ferris, Jennifer ;
Buckley, Niamh E. ;
Coulter, Paula ;
McCabe, Nuala ;
Eddie, Sharon L. ;
Dunne, Philip D. ;
O'Reilly, Paul ;
Gilmore, Alan ;
Feeney, Laura ;
Ewing, David Lyons ;
Drapkin, Ronny, I ;
Salto-Tellez, Manuel ;
Kennedy, Richard D. ;
Harley, Ian J. G. ;
McCluggage, W. Glenn ;
Mullan, Paul B. .
GYNECOLOGIC ONCOLOGY, 2019, 155 (02) :305-317
[8]   POTE paralogs are induced and differentially expressed in many cancers [J].
Bera, TK ;
Fleur, AS ;
Lee, Y ;
Kydd, A ;
Hahn, K ;
Popescu, NC ;
Zimonjic, DB ;
Lee, B ;
Pastan, I .
CANCER RESEARCH, 2006, 66 (01) :52-56
[9]   Evaluation of Attenuated Tumor Antigens and the Implications for Peptide-Based Cancer Vaccine Development [J].
Berry, J. S. ;
Vreeland, T. J. ;
Hale, D. F. ;
Jackson, D. O. ;
Trappey, A. F. ;
Greene, J. M. ;
Hardin, M. O. ;
Herbert, G. S. ;
Clifton, G. T. ;
Peoples, G. E. .
JOURNAL OF CANCER, 2017, 8 (07) :1255-1262
[10]   Regulation of cytotoxic T-cell responses by p53 in cancer [J].
Braun, Mitchell W. ;
Iwakuma, Tomoo .
TRANSLATIONAL CANCER RESEARCH, 2016, 5 (06) :692-697