Antiproliferative Effects of Recombinant Apoptin on Lung and Breast Cancer Cell Lines

被引:1
作者
Razliqi, Masoud Ezami [1 ]
Olad, Gholamreaza [2 ]
Dorostkar, Rouhollah [1 ]
Heydari, Sahar [2 ]
Ghaleh, Hadi Esmaeili Gouvarchin [1 ]
机构
[1] Baqiyatallah Univ Med Sci, Appl Virol Res Ctr, Tehran, Iran
[2] Baqiyatallah Univ Med Sci, Appl Biotechnol Res Ctr, Tehran, Iran
关键词
Breast cancer; Chicken anemia virus; Lung cancer; Oncolytic virotherapy; Recombinant apoptin; TRANSFORMATION;
D O I
10.34172/aim.2020.69
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Selective therapy has always been the main challenge in cancer treatments. Various non-replicative oncolytic viral systems have revealed the safety and efficacy of using viruses and these products. The aim of this paper is to examine the impact of recombinant apoptin on the proliferation of lung cancer and breast cancer cell lines. Methods: The present study consisted of two steps of expression of recombinant apoptin and its anti-proliferative effects on normal and cancer cells. In the first step, following bioinformatics and optimizing apoptin gene sequencing and synthesis, it was expressed using vector PET28a and E. coli BL21 (DE3). The expressed recombinant apoptin was confirmed by analytical SDSPAGE and then purified using Ni affinity chromatography. In the second step, the antiproliferative effects of recombinant apoptin on lung cancer, breast cancer and primary cell lines were determined using MTT assay. Results: According to the results of SDS-PAGE gel assay, recombinant apoptin was visible in the 14 kDa band. Also, the MTT assay results indicated that the antiproliferative effects of recombinant apoptin in cancer cell lines was different compared with the primary cell line, and followed a dose-dependent manner in both cell lines. The highest cytotoxicity (lowest cell viability) groups were 0.2 mg/mL in lung cancer (0.32 +/- 0.015) (P<0.001), and in breast cancer (0.33 +/- 0.031) (P<0.001) and 0.032 mg/mL in primary cells (0.17 +/- 0.004) (P<0.01), as compared to the control groups. Conclusion: Our results confirmed that recombinant apoptin can induce antiproliferative effects in lung cancer and breast cancer cell lines, but not in normal monkey kidney cell line Vero; thus, it can be introduced as a promising novel specific antitumor agent after further evaluation in clinical trials.
引用
收藏
页码:593 / 599
页数:7
相关论文
共 30 条
[1]   Human Gyrovirus Apoptin as a Potential Selective Anticancer Agent: An In Vitro Study [J].
Akbari, Amir ;
Arabsolghar, Rita ;
Behbahani, Abbas Behzad ;
Dehbidi, Gholamreza Rafiei ;
Zare, Farahnaz ;
Hadi, Mandeih .
PHARMACEUTICAL SCIENCES, 2019, 25 (01) :44-49
[2]   Therapeutic Potential of Nanoparticle-loaded Hydroxyurea on Proliferation of Human Breast Adenocarcinoma Cell Line [J].
Azemati, Fateme ;
Kondori, Bahman Jalali ;
Ghaleh, Hadi Esmaeili Gouvarchin .
IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH, 2020, 19 (01) :271-281
[3]   Polyplexes of Functional PAMAM Dendrimer/Apoptin Gene Induce Apoptosis of Human Primary Glioma Cells In Vitro [J].
Bae, Yoonhee ;
Le Thi Thuy ;
Lee, Young Hwa ;
Ko, Kyung Soo ;
Han, Jin ;
Choi, Joon Sig .
POLYMERS, 2019, 11 (02)
[4]   Recombinant adenoviruses expressing apoptin suppress the growth of MCF-7 breast cancer cells and affect cell autophagy [J].
Chen, Shuang ;
Li, Yi-Quan ;
Yin, Xun-Zhe ;
Li, Shan-Zhi ;
Zhu, Yi-Long ;
Fan, Yuan-Yuan ;
Li, Wen-Jie ;
Cui, Ying-Li ;
Zhao, Jin ;
Li, Xiao ;
Zhang, Qing-Gao ;
Jin, Ning-Yi .
ONCOLOGY REPORTS, 2019, 41 (05) :2818-2832
[5]   Identification of nuclear localization signal and nuclear export signal of VP1 from the chicken anemia virus and effects on VP2 shuttling in cells [J].
Cheng, Jai-Hong ;
Lai, Guan-Hua ;
Lien, Yi-Yang ;
Sun, Fang-Chun ;
Hsu, Shan-Ling ;
Chuang, Pei-Chin ;
Lee, Meng-Shiou .
VIROLOGY JOURNAL, 2019, 16 (1)
[6]   Functionalized Tobacco Mosaic Virus Coat Protein Monomers and Oligomers as Nanocarriers for Anti-Cancer Peptides [J].
Gamper, Coralie ;
Spenle, Caroline ;
Bosca, Sonia ;
van der Heyden, Michael ;
Erhardt, Mathieu ;
Orend, Gertraud ;
Bagnard, Dominique ;
Heinlein, Manfred .
CANCERS, 2019, 11 (10)
[7]   Cell-Free Nucleic Acids Circulating in the Plasma of Colorectal Cancer Patients Induce the Oncogenic Transformation of Susceptible Cultured Cells [J].
Garcia-Olmo, Dolores C. ;
Dominguez, Carolina ;
Garcia-Arranz, Mariano ;
Anker, Phillipe ;
Stroun, Maurice ;
Garcia-Verdugo, Jose M. ;
Garcia-Olmo, Damian .
CANCER RESEARCH, 2010, 70 (02) :560-567
[8]   Using CuO nanoparticles and hyperthermia in radiotherapy of MCF-7 cell line: synergistic effect in cancer therapy [J].
Ghaleh, Hadi Esmaeili Govarchin ;
Zarei, Leila ;
Motlagh, Bahman Mansori ;
Jabbari, Nasrollah .
ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY, 2019, 47 (01) :1396-1403
[9]   Methylation of HPV 16 and EPB41L3 in oral gargles: Associations with oropharyngeal cancer detection and tumor characteristics [J].
Giuliano, Anna R. ;
Nedjai, Belinda ;
Lorincz, Attila T. ;
Schell, Michael J. ;
Rahman, Shams ;
Banwait, Rawinder ;
Boulware, David ;
Sirak, Bradley ;
Martin-Gomez, Laura ;
Abrahamsen, Martha ;
Isaacs-Soriano, Kimberly A. ;
Wenig, Bruce ;
Chung, Christine H. ;
Caudell, Jimmy .
INTERNATIONAL JOURNAL OF CANCER, 2020, 146 (04) :1018-1030
[10]   Assessment of synergistic effect of combining hyperthermia with irradiation and calcium carbonate nanoparticles on proliferation of human breast adenocarcinoma cell line (MCF-7 cells) [J].
Jabbari, Nasrollah ;
Zarei, Leila ;
Galeh, Hadi Esmaeili Govarchin ;
Motlagh, Bahman Mansori .
ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY, 2018, 46 :364-372