| Literature DB >> 25799942 |
Shannon D McClintock1, Roscoe L Warner, Saqib Ali, Apurupa Chekuri, Michael K Dame, Durga Attili, Randall K Knibbs, Muhammad Nadeem Aslam, Joseph Sinkule, Alton Charles Morgan, Adel Barsoum, Lauren B Smith, David G Beer, Kent J Johnson, James Varani.
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.Entities:
Keywords: A20 murine B-cell leukemia; ADC, Antibody-drug conjugate; ADCC, Antibody dependent cellular cytotoxicity; ANOVA, Analysis of variance; B16 melanoma; BV, Benovus; CDC, Complement dependent cytotoxicity; ELISA, Enzyme-linked immunosorbent assay; FBS, Fetal bovine serum; IgG, Immunoglobulin G; LRP, Laminin receptor protein; OFA/iLRP, Oncofetal antigen –; RPMI, Roswell Park Memorial Institute; SCID, Severe combined immune deficiency; blood-borne metastasis; cDNA, complementary DNA; immature laminin receptor protein; kD, kilo Dalton; mRNA, messenger RNA
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Year: 2015 PMID: 25799942 PMCID: PMC4622506 DOI: 10.1080/15384047.2015.1026484
Source DB: PubMed Journal: Cancer Biol Ther ISSN: 1538-4047 Impact factor: 4.742