4.4 Article

Preclinical studies with JAA-F11 anti-Thomsen-Friedenreich monoclonal antibody for human breast cancer

Journal

FUTURE ONCOLOGY
Volume 10, Issue 3, Pages 385-399

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/FON.13.209

Keywords

enzyme immunoassay; human breast cancer cell lines; JAA-F11 monoclonal antibody; monoclonal antibody; Thomsen-Friedenreich antigen

Categories

Funding

  1. NIH STTR
  2. CDMRP [W81XWH-04-1-0342]
  3. Oncologic Foundation of Buffalo
  4. UB STOR Product Development Fund
  5. Oishei Foundation
  6. Bruce Holm Catalyst Fund
  7. Mark Diamond Research Foundation of the State University of New York at Buffalo [SP-11-05]
  8. Mark Diamond Research Foundation
  9. Organization of American States
  10. National Cancer Institute [NIH 1 R41 CA176951-01]
  11. Bruce Holm Memorial Catalyst Fund
  12. NSF [1204209]
  13. NIAID [R15 AI 49210-01]
  14. Direct For Education and Human Resources
  15. Division Of Undergraduate Education [1204209] Funding Source: National Science Foundation

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Aim: The Thomsen-Friedenreich antigen (TF-Ag) is a disaccharide hidden on normal cells, but selectively exposed on the surface of breast, colon, prostate and bladder cancer cells. JAA-F11, a highly specific monoclonal antibody to TF-Ag, reduces metastasis and prolongs survival in a mouse model. In addition,I-124-JAA-F11 localizes 4T1 tumors in mice. These studies continue translation of JAA-F11 to human breast cancer. Materials & methods & results: Of the 41 human breast cancer cell lines tested, 78% were positive for reactivity with JAA-F11 by whole-cell enzyme immunoassay and positivity occurred unrelated to estrogen, progesterone or HER2 receptor status. JAA-F11 inhibited the growth rate of the human cancer cell lines tested. At 1 h, approximately 80% of JAA-F11 internalized in the three cell lines tested. I-124-JAA-F11 specifically imaged human triple-negative tumors in mice by microPET. Conclusion: The results highlight the potential that humanized JAA-F11 may have for immunotherapy and drug conjugate therapy in breast cancer patients.

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