AI Article Synopsis

  • The study investigates the effectiveness of two mouse monoclonal antibodies targeting the oncofetal antigen immature laminin receptor protein (OFA/iLRP) in suppressing tumor growth and metastasis in leukemia and melanoma models.
  • The antibodies showed modest success in preventing tumor growth at the original site but significantly reduced tumor formation in other organs after tumor cells were injected into the bloodstream.
  • These findings indicate that anti-OFA/iLRP antibodies may serve as a potential therapy for patients with leukemia and could also be beneficial in treating solid tumors with metastatic spread.

Article Abstract

The oncofetal antigen - immature laminin receptor protein (OFA/iLRP) has been linked to metastatic tumor spread for several years. The present study, in which 2 highly-specific, high-affinity OFA/iLRP-reactive mouse monoclonal antibodies were examined for ability to suppress tumor cell growth and metastatic spread in the A20 B-cell leukemia model and the B16 melanoma model, provides the first direct evidence that targeting OFA/iLRP with exogenous antibodies can have therapeutic benefit. While the antibodies were modestly effective at preventing tumor growth at the primary injection site, both antibodies strongly suppressed end-organ tumor formation following intravenous tumor cell injection. Capacity of anti-OFA/iLRP antibodies to suppress tumor spread through the blood in the leukemia model suggests their use as a therapy for individuals with leukemic disease (either for patients in remission or even as part of an induction therapy). The results also suggest use against metastatic spread with solid tumors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4622506PMC
http://dx.doi.org/10.1080/15384047.2015.1026484DOI Listing

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