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BAMLET Administration Via Drinking Water Inhibits Intestinal Tumor Development and Promotes Long-term Health

Overview
Journal Sci Rep
Specialty Science
Date 2024 Feb 15
PMID 38360830
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Abstract

Though new targeted therapies for colorectal cancer, which progresses from local intestinal tumors to metastatic disease, are being developed, tumor specificity remains an important problem, and side effects a major concern. Here, we show that the protein-fatty acid complex BAMLET (bovine alpha-lactalbumin made lethal to tumor cells) can act as a peroral treatment for colorectal cancer. Apc mice, which carry mutations relevant to hereditary and sporadic human colorectal cancer, that received BAMLET in the drinking water showed long-term protection against tumor development and decreased expression of tumor growth-, migration-, metastasis- and angiogenesis-related genes. BAMLET treatment via drinking water inhibited the Wnt/β-catenin and PD-1 signaling pathways and prolonged survival without evidence of toxicity. Systemic disease in the lungs, livers, spleens, and kidneys, which accompanied tumor progression, was inhibited by BAMLET treatment. The metabolic response to BAMLET included carbohydrate and lipid metabolism, which were inhibited in tumor prone Apc mice and weakly regulated in C57BL/6 mice, suggesting potential health benefits of peroral BAMLET administration in addition to the potent antitumor effects. Together, these findings suggest that BAMLET administration in the drinking water maintains antitumor pressure by removing emergent cancer cells and reprogramming gene expression in intestinal and extra-intestinal tissues.

References
1.
Sung H, Ferlay J, Siegel R, Laversanne M, Soerjomataram I, Jemal A . Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021; 71(3):209-249. DOI: 10.3322/caac.21660. View

2.
Vogelstein B, Fearon E, Hamilton S, Kern S, Preisinger A, Leppert M . Genetic alterations during colorectal-tumor development. N Engl J Med. 1988; 319(9):525-32. DOI: 10.1056/NEJM198809013190901. View

3.
McCart A, Vickaryous N, Silver A . Apc mice: models, modifiers and mutants. Pathol Res Pract. 2008; 204(7):479-90. DOI: 10.1016/j.prp.2008.03.004. View

4.
Moser A, Pitot H, Dove W . A dominant mutation that predisposes to multiple intestinal neoplasia in the mouse. Science. 1990; 247(4940):322-4. DOI: 10.1126/science.2296722. View

5.
Mok K, Nagashima T, Day I, Hore P, Dobson C . Multiple subsets of side-chain packing in partially folded states of alpha-lactalbumins. Proc Natl Acad Sci U S A. 2005; 102(25):8899-904. PMC: 1157025. DOI: 10.1073/pnas.0500661102. View