Inhibition of breast cancer xenografts in a mouse model and the induction of apoptosis in multiple breast cancer cell lines by lactoferricin B peptide.
Rizdwan RahmanAlyssa Danielle FonsekaShiang-Chia SuaMunirah AhmadRamkumar RajendranStephen AmbuFabian Davamani AmalrajAlan Soo-Beng KhooEbenezer ChitraPublished in: Journal of cellular and molecular medicine (2021)
Breast cancer has a diverse aetiology characterized by the heterogeneous expression of hormone receptors and signalling molecules, resulting in varied sensitivity to chemotherapy. The adverse side effects of chemotherapy coupled with the development of drug resistance have prompted the exploration of natural products to combat cancer. Lactoferricin B (LfcinB) is a natural peptide derived from bovine lactoferrin that exhibits anticancer properties. LfcinB was evaluated in vitro for its inhibitory effects on cell lines representing different categories of breast cancer and in vivo for its suppressive effects on tumour xenografts in NOD-SCID mice. The different breast cancer cell lines exhibited varied levels of sensitivity to apoptosis induced by LfcinB in the order of SKBR3>MDA-MB-231>MDA-MB-468>MCF7, while the normal breast epithelial cells MCF-10A were not sensitive to LfcinB. The peptide also inhibited the invasion of the MDA-MB-231 and MDA-MB-468 cell lines. In the mouse xenograft model, intratumoural injections of LfcinB significantly reduced tumour growth rate and tumour size, as depicted by live imaging of the mice using in vivo imaging systems (IVIS). Harvested tumour volume and weight were significantly reduced by LfcinB treatment. LfcinB, therefore, is a promising and safe candidate that can be considered for the treatment of breast cancer.
Keyphrases
- breast cancer cells
- cell cycle arrest
- mouse model
- oxidative stress
- cell death
- endoplasmic reticulum stress
- type diabetes
- body mass index
- mass spectrometry
- young adults
- breast cancer risk
- locally advanced
- metabolic syndrome
- ultrasound guided
- weight loss
- pi k akt
- combination therapy
- signaling pathway
- chemotherapy induced