HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The translation elongation factor eEF2 is a novel tumor‑associated antigen overexpressed in various types of cancers.

Abstract
Recent studies have shown that cancer immunotherapy could be a promising therapeutic approach for the treatment of cancer. In the present study, to identify novel tumor-associated antigens (TAAs), the proteins expressed in a panel of cancer cells were serologically screened by immunoblot analysis and the eukaryotic elongation factor 2 (eEF2) was identified as an antigen that was recognized by IgG autoantibody in sera from a group of patients with head and neck squamous cell carcinoma (HNSCC) or colon cancer. Enzyme-linked immunosorbent assay showed that serum eEF2 IgG Ab levels were significantly higher in colorectal and gastric cancer patients compared to healthy individuals. Immunohistochemistry experiments showed that the eEF2 protein was overexpressed in the majority of lung, esophageal, pancreatic, breast and prostate cancers, HNSCC, glioblastoma multiforme and non-Hodgkin's lymphoma (NHL). Knockdown of eEF2 by short hairpin RNA (shRNA) significantly inhibited the growth in four eEF2-expressing cell lines, PC14 lung cancer, PCI6 pancreatic cancer, HT1080 fibrosarcoma and A172 glioblastoma cells, but not in eEF2-undetectable MCF7 cells. Furthermore, eEF2-derived 9-mer peptides, EF786 (eEF2 786-794 aa) and EF292 (eEF2 292-300 aa), elicited cytotoxic T lymphocyte (CTL) responses in peripheral blood mononuclear cells (PBMCs) from an HLA-A*24:02- and an HLA-A*02:01-positive healthy donor, respectively, in an HLA-A-restricted manner. These results indicated that the eEF2 gene is overexpressed in the majority of several types of cancers and plays an oncogenic role in cancer cell growth. Moreover, the eEF2 gene product is immunogenic and a promising target molecule of cancer immunotherapy for several types of cancers.
AuthorsYusuke Oji, Naoya Tatsumi, Mari Fukuda, Shin-Ichi Nakatsuka, Sayaka Aoyagi, Erika Hirata, Isamu Nanchi, Fumihiro Fujiki, Hiroko Nakajima, Yumiko Yamamoto, Syohei Shibata, Michiyo Nakamura, Kana Hasegawa, Sayaka Takagi, Ikuyo Fukuda, Tomoko Hoshikawa, Yui Murakami, Masahide Mori, Masayoshi Inoue, Tetsuji Naka, Takeshi Tomonaga, Yoshifumi Shimizu, Masashi Nakagawa, Junichi Hasegawa, Riichiro Nezu, Hidenori Inohara, Shuichi Izumoto, Norio Nonomura, Toshiki Yoshimine, Meinoshin Okumura, Eiichi Morii, Hajime Maeda, Sumiyuki Nishida, Naoki Hosen, Akihiro Tsuboi, Yoshihiro Oka, Haruo Sugiyama
JournalInternational journal of oncology (Int J Oncol) Vol. 44 Issue 5 Pg. 1461-9 (May 2014) ISSN: 1791-2423 [Electronic] Greece
PMID24589652 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, Neoplasm
  • Immunoglobulin G
  • Elongation Factor 2 Kinase
Topics
  • Antigens, Neoplasm (genetics, metabolism)
  • Cell Line, Tumor
  • Elongation Factor 2 Kinase (genetics, metabolism)
  • Gene Expression Regulation, Neoplastic
  • Gene Knockdown Techniques
  • Humans
  • Immunoglobulin G (immunology)
  • MCF-7 Cells
  • Neoplasms (genetics, immunology, pathology)
  • Sequence Analysis, DNA
  • T-Lymphocytes, Cytotoxic (immunology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: