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Estudio2015

A red meat-derived glycan promotes inflammation and cancer progression

Samraj AN, Pearce OM, Läubli H, Crittenden AN, Bergfeld AK, Banda K, Gregg CJ, Bingman AE, Secrest P, Diaz SL, Varki NM, Varki A

Proceedings of the National Academy of Sciences of the United States of America · 297 citas

Cómo se estudió

Diseño
Estudio en animales (clasificado por nuestro filtro de IA)
Estudiado en
Animales
Resultado principal
Eventos clínicos como enfermedad o muerte

Quién lo pagó

Financiación
Financiación independiente
Gobierno
National Science Foundation
Organización sin fines de lucro
Ellison Medical Foundation
Organización sin fines de lucro
Cancer Research Institute
Universidad u hospital
Harvard University
Universidad u hospital
University of Cambridge
Gobierno
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Gobierno
National Institutes of Health
Gobierno
National Cancer Institute
Gobierno
National Institute of Diabetes and Digestive and Kidney Diseases
Gobierno
NIH HHS
Gobierno
NIDDK NIH HHS
Gobierno
NCI NIH HHS
Gobierno
HHS | NIH | National Cancer Institute
Subvenciones
National Cancer Institute (R01 CA 38701); National Institute of Diabetes and Digestive and Kidney Diseases (T32 DK 069263); National Cancer Institute (R01 CA038701); National Institutes of Health (P51‐OD011132); National Institutes of Health (R01 CA38701)

Según 13 financiadores declarados.

Publicación

Publicado
2014-12-29 · Proc Natl Acad Sci U S A · vol. 112 · número 2 · págs. 542–547
Editorial
National Academy of Sciences
Citado
408 citas · más que el 100% de estudios similares · 45.1× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
68 trabajos
Acceso
Lectura gratuita
Áreas de investigación
Milk Quality and Mastitis in Dairy Cows · melanin and skin pigmentation · Glycosylation and Glycoproteins Research
Palabras clave
Inflammation, Red meat, Sialic acid, Cancer, Biology, Immunology, Medicine, Internal medicine, Food science, Biochemistry
MeSH
animals, mice, congenic, mice, inbred c57bl, mice, knockout, humans, mice, liver neoplasms, experimental, disease progression, inflammation, neuraminic acids, n-acetylneuraminic acid, mixed function oxygenases, antibodies, blocking, risk factors, food analysis, meat, male

12 autores

  • Annie N. Samraj🇺🇸University of California San Diego
  • Oliver M.T. Pearce🇺🇸University of California San Diego
  • Heinz Philipp Laubli🇺🇸University of California San Diego
  • Alyssa N. Crittenden🇺🇸University of California San Diego
  • Anne K. Bergfeld🇺🇸University of California San Diego
  • Kalyan Banda🇺🇸University of California San Diego
  • Christopher Gregg🇺🇸University of California San Diego
  • Andrea E. Bingman🇺🇸University of California San Diego
  • Patrick Secrest🇺🇸University of California San Diego
  • Sandra L. Diaz🇺🇸University of California San Diego
  • Nissi M. Varki🇺🇸University of California San Diego
  • Ajit P Varki🇺🇸University of California San Diego

Resumen

El texto original del estudio, en el idioma en que se publicó.

A well known, epidemiologically reproducible risk factor for human carcinomas is the long-term consumption of "red meat" of mammalian origin. Although multiple theories have attempted to explain this human-specific association, none have been conclusively proven. We used an improved method to survey common foods for free and glycosidically bound forms of the nonhuman sialic acid N-glycolylneuraminic acid (Neu5Gc), showing that it is highly and selectively enriched in red meat. The bound form of Neu5Gc is bioavailable, undergoing metabolic incorporation into human tissues, despite being a foreign antigen. Interactions of this antigen with circulating anti-Neu5Gc antibodies could potentially incite inflammation. Indeed, when human-like Neu5Gc-deficient mice were fed bioavailable Neu5Gc and challenged with anti-Neu5Gc antibodies, they developed evidence of systemic inflammation. Such mice are already prone to develop occasional tumors of the liver, an organ that can incorporate dietary Neu5Gc. Neu5Gc-deficient mice immunized against Neu5Gc and fed bioavailable Neu5Gc developed a much higher incidence of hepatocellular carcinomas, with evidence of Neu5Gc accumulation. Taken together, our data provide an unusual mechanistic explanation for the epidemiological association between red meat consumption and carcinoma risk. This mechanism might also contribute to other chronic inflammatory processes epidemiologically associated with red meat consumption.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial.

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