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Docosahexaenoic acid suppresses breast cancer cell metastasis by targeting matrix-metalloproteinases

Yun EJ, Song KS, Shin S, Kim S, Heo JY, Kweon GR, Wu T, Park JI, Lim K

Oncotarget · 34 citas

Cómo se estudió

Diseño
Estudio in vitro o de mecanismos (clasificado por nuestro filtro de IA)
Estudiado en
Personas, más trabajo en animales o laboratorio
Resultado principal
Eventos clínicos como enfermedad o muerte

Quién lo pagó

Financiación
Financiación independiente
Gobierno
National Research Foundation
Universidad u hospital
Chungnam National University
Gobierno
Ministry of Science, ICT and Future Planning
Gobierno
National Research Foundation of Korea

Según 4 financiadores declarados.

Publicación

Publicado
2016-06-23 · Oncotarget · vol. 7 · número 31 · págs. 49961–49971
Editorial
Impact Journals LLC
Citado
47 citas · más que el 82% de estudios similares · 1.7× el promedio de su campo
Referencias
54 trabajos
Acceso
Acceso abierto (publicación gratuita) · CC-BY
Áreas de investigación
Cancer, Lipids, and Metabolism · Inflammatory mediators and NSAID effects · Fatty Acid Research and Health
Palabras clave
Breast cancer, Metastasis, Cancer research, Docosahexaenoic acid, Medicine, Metastatic breast cancer, Matrix metalloproteinase, Cancer, Lung cancer, In vivo, Internal medicine, Oncology, Biology, Fatty acid, Polyunsaturated fatty acid
MeSH
cell line, tumor, animals, mice, inbred c57bl, mice, transgenic, humans, mice, breast neoplasms, neoplasm invasiveness, neoplasm metastasis, disease progression, docosahexaenoic acids, dinoprostone, nf-kappa b, culture media, conditioned, apoptosis, cell proliferation, cell movement, cell survival, gene expression regulation, neoplastic, active transport, cell nucleus, female, cyclooxygenase 2, matrix metalloproteinase 2, matrix metalloproteinase 9, matrix metalloproteinase inhibitors

9 autores

  • Eun-Jin Yun🇰🇷🇺🇸 · autor de correspondenciaChungnam National University; The University of Texas Southwestern Medical Center
  • Kyung-Sub Song🇺🇸🇰🇷 · autor de correspondenciaTulane University; Chungnam National University
  • Soyeon Shin🇰🇷Chungnam National University
  • Soyeon Kim🇰🇷Chungnam National University
  • Jun Young Heo🇰🇷Chungnam National University
  • Gi‐Ryang Kweon🇰🇷Chungnam National University
  • Tong Wu🇺🇸Tulane University
  • Jong‐Il Park🇰🇷Chungnam National University
  • Kyu Lim🇰🇷Chungnam National University

Resumen

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

Breast cancer is one of the most prevalent cancers in women, and nearly half of breast cancer patients develop distant metastatic disease after therapy. Despite the significant advances that have been achieved in understanding breast cancer metastasis in the past decades, metastatic cancer is still hard to cure. Here, we demonstrated an anti-cancer mechanism of docosahexaenoic acid (DHA) that suppressed lung metastasis in breast cancer. DHA could inhibit proliferation and invasion of breast cancer cells in vitro, and this was mainly through blocking Cox-2-PGE2-NF-κB-MMPs cascades. DHA treatment significantly decreased Cox-2 and NF-κB expression as well as nuclear translocation of NF-κB in MDA-MB-231 cells. In addition, DHA also reduced NF-κB binding to DNA which may lead to inactivation of MMPs. Moreover, in vivo studies using Fat-1 transgenic mice showed remarkable decrease of tumor growth and metastasis to EO771 cells to lung in DHA-rich environment. In conclusion, DHA attenuated breast cancer progression and lung metastasis in part through suppressing MMPs, and these findings suggest chemoprevention and potential therapeutic strategy to overcome malignant breast cancer.

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

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