Antiproliferative and Apoptotic Effects of Novel Anti-ROR1 Single-Chain Antibodies in Hematological Malignancies

被引:23
作者
Aghebati-Maleki, Leili [1 ,2 ,3 ,4 ]
Younesi, Vahid [5 ,6 ]
Baradaran, Behzad [1 ,4 ]
Abdolalizadeh, Jalal [1 ]
Motallebnezhad, Morteza [1 ,2 ,4 ]
Nickho, Hamid [1 ,2 ,4 ]
Shanehbandi, Dariush [1 ]
Majidi, Jafar [1 ,4 ]
Yousefi, Mehdi [2 ,4 ]
机构
[1] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Student Res Comm, Tabriz, Iran
[4] Tabriz Univ Med Sci, Sch Med, Dept Immunol, Tabriz, Iran
[5] Alborz Univ Med Sci, Fac Paramed Sci, Karaj, Iran
[6] Pishtaz Teb Zaman Diagnost, Tehran, Iran
关键词
ROR1; phage display; scFv; hematological malignancies; immunotherapy; CHRONIC LYMPHOCYTIC-LEUKEMIA; TYROSINE KINASE ROR1; BREAST-CANCER CELLS; PHAGE DISPLAY; ANTIGEN ROR1; CLL CELLS; RECEPTOR; EXPRESSION; GENERATION; LIBRARIES;
D O I
10.1177/2472555216689659
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Receptor tyrosine kinase-like orphan receptor (ROR) proteins are a conserved family of tyrosine kinase receptors that function in developmental processes including cell survival, differentiation, cell migration, cell communication, cell polarity, proliferation, metabolism, and angiogenesis. ROR1 has recently been shown to be expressed in various types of cancer cells but not normal cells. Pharmacokinetics and pharmacodynamics of single-chain Fragment variable (scFv) antibodies provide potential therapeutic advantages over whole antibody molecules. In the present study, scFvs against a specific peptide from the extracellular domain of ROR1 were selected using phage display technology. The selected scFvs were further characterized using polyclonal and monoclonal phage enzyme-linked immunosorbent assay (ELISA), soluble monoclonal ELISA, colony PCR, and sequencing. Antiproliferative and apoptotic effects of selected scFv antibodies were also evaluated in lymphoma and myeloma cancer cell lines using MTT and annexin V/PI assays. The results of ELISA indicated specific reactions of the isolated scFvs against the ROR1 peptide. Colony PCR confirmed the presence of full-length V-H and V kappa inserts. The percentages of cell growth after 24 h of treatment of cells with individual scFv revealed that the scFv significantly inhibited the growth of the RPMI8226 and chronic lymphocytic leukemia (CLL) cells in comparison with the untreated cells (p < 0.05). Interestingly, 24-h treatment with specific scFv induced apoptosis cell death in the RPMI8226 and CLL cells. Taken together, our results demonstrate that targeting of ROR1 using peptide-specific scFv can be an effective immunotherapy strategy in hematological malignancies.
引用
收藏
页码:408 / 417
页数:10
相关论文
共 31 条
[1]   Phage display as a promising approach for vaccine development [J].
Aghebati-Maleki, Leili ;
Bakhshinejad, Babak ;
Baradaran, Behzad ;
Motallebnezhad, Morteza ;
Aghebati-Maleki, Ali ;
Nickho, Hamid ;
Yousefi, Mehdi ;
Majidi, Jafar .
JOURNAL OF BIOMEDICAL SCIENCE, 2016, 23
[2]   Unique cell surface expression of receptor tyrosine kinase ROR1 in human B-cell chronic lymphocytic leukemia [J].
Baskar, Sivasubramanian ;
Kwong, Kayin ;
Hofer, Thomas ;
Levy, Jessica M. ;
Kennedy, Michael G. ;
Lee, Elinor ;
Staudt, Louis M. ;
Wilson, Wyndham H. ;
Wiestner, Adrian ;
Rader, Christoph .
CLINICAL CANCER RESEARCH, 2008, 14 (02) :396-404
[3]   Phage displaya powerful technique for immunotherapy 1. Introduction and potential of therapeutic applications [J].
Bazan, Justyna ;
Calkosinski, Ireneusz ;
Gamian, Andrzej .
HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2012, 8 (12) :1817-1828
[4]   ROR1, an embryonic protein with an emerging role in cancer biology [J].
Borcherding, Nicholas ;
Kusner, David ;
Liu, Guang-Hui ;
Zhang, Weizhou .
PROTEIN & CELL, 2014, 5 (07) :496-502
[5]   Silencing of ROR1 and FMOD with siRNA results in apoptosis of CLL cells [J].
Choudhury, Aniruddha ;
Derkow, Katja ;
Daneshmanesh, Amir Hossein ;
Mikaelsson, Eva ;
Kiaii, Shahryar ;
Kokhaei, Parviz ;
Osterborg, Anders ;
Mellstedt, Hakan .
BRITISH JOURNAL OF HAEMATOLOGY, 2010, 151 (04) :327-335
[6]   Targeting ROR1 Inhibits Epithelial-Mesenchymal Transition and Metastasis [J].
Cui, Bing ;
Zhang, Suping ;
Chen, Liguang ;
Yu, Jianqiang ;
Widhopf, George F., II ;
Fecteau, Jessie-F. ;
Rassenti, Laura Z. ;
Kipps, Thomas J. .
CANCER RESEARCH, 2013, 73 (12) :3649-3660
[7]   Monoclonal antibodies against ROR1 induce apoptosis of chronic lymphocytic leukemia (CLL) cells [J].
Daneshmanesh, A. H. ;
Hojjat-Farsangi, M. ;
Khan, A. S. ;
Jeddi-Tehrani, M. ;
Akhondi, M. M. ;
Bayat, A. A. ;
Ghods, R. ;
Mahmoudi, A-R ;
Hadavi, R. ;
Osterborg, A. ;
Shokri, F. ;
Rabbani, H. ;
Mellstedt, H. .
LEUKEMIA, 2012, 26 (06) :1348-1355
[8]   The PI3K/AKT/mTOR pathway is involved in direct apoptosis of CLL cells induced by ROR1 monoclonal antibodies [J].
Daneshmanesh, Amir Hossein ;
Hojjat-Farsangi, Mohammad ;
Moshfegh, Ali ;
Khan, Abdul Salam ;
Mikaelsson, Eva ;
Osterborg, Anders ;
Mellstedt, Hakan .
BRITISH JOURNAL OF HAEMATOLOGY, 2015, 169 (03) :455-458
[9]   Orphan receptor tyrosine kinases ROR1 and ROR2 in hematological malignancies [J].
Daneshmanesh, Amir Hossein ;
Porwit, Anna ;
Hojjat-Farsangi, Mohammad ;
Jeddi-Tehrani, Mahmood ;
Tamm, Katja Pokrovskaja ;
Grander, Dan ;
Lehmann, Soren ;
Norin, Stefan ;
Shokri, Fazel ;
Rabbani, Hodjattallah ;
Mellstedt, Hakan ;
Osterborg, Anders .
LEUKEMIA & LYMPHOMA, 2013, 54 (04) :843-850
[10]   A C-elegans Ror receptor tyrosine kinase regulates cell motility and asymmetric cell division [J].
Forrester, WC ;
Dell, M ;
Perens, E ;
Garriga, G .
NATURE, 1999, 400 (6747) :881-885