4.6 Article

Preparation and identification of anti-breast cancer cells peptides released from yak milk casein

Journal

FRONTIERS IN NUTRITION
Volume 9, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnut.2022.997514

Keywords

hydrolysate; peptides; breast cancer cells; yak milk casein; identification

Funding

  1. National Natural Science Foundation of China [31871806]
  2. Beijing Dairy Industry Innovation Team [BAIC06-2022]
  3. Scientific Research Plan Projects of Shaanxi Education Department, China [21JK0469]
  4. Natural Science Foundation of Shaanxi Province [2020JM-628]
  5. Senior Talent Foundation of An Kang University, China [2021AYQDZR04]
  6. Crosswise Research Foundation of An Kang University, China [2017AYHX021]

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This study identified anti-breast cancer peptides from yak milk casein (YMC) and evaluated their inhibitory effects on cancer cells. A nonapeptide (TPVVVPPFL) showed potent inhibitory effects on cancer cells and exhibited good gastrointestinal stability.
Yak milk casein (YMC) is the main protein in the yak milk. Peptides released from Yak milk casein (YMC) have multiple bioactivities, including anti-inflammation and immune-regulation, suggesting that these peptides might be able to inhibit cancer theoretically. However, the anti-cancer peptides from YMC have only been sparsely studied. Breast carcinoma is the most common carcinoma in women worldwide. Thus, the paper herein was to identify yak milk casein (YMC)-derived anti-breast cancer peptides via gel filtration, reversed phase high-performance liquid chromatography (RP-HPLC) and liquid chromatography electrospray ionization tandem mass spectrometry (LC-ESI MS/MS) for the first time. The inhibitory effects of the hydrolysates on the cell viabilities, cell cycles and apoptosis of breast cancer cells were evaluated with a cck8 kit and a flow cytometry. The result showed that YMC hydrolysates (YMCH) obtained by united hydrolyzation with trypsin (3 h) and alkaline protease (3 h) displayed the highest cell viability inhibition rate for MCF7 (20.74 +/- 1.39%) and MDA-MB-231 (26.73 +/- 2.87%) cells. Three peptides were identified in the RP-HPLC subfraction F3-4, and a nonapeptide (TPVVVPPFL) showed the most potent inhibitory effects on both cancer cells and displayed good gastrointestinal stability. TPVVVPPFL could induce G2-M cell cycle arrest in MCF7 cells and S cell arrest in MDA-MB-231 cells and induce apoptosis in both cancer cells. Moreover, in silico analysis indicated that the peptide had non-toxic and no inhibitory roles on P4502D6-enzyme. Together, this study shows that YMC is a good source of anti-breast cancer cells peptides.

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