The anticancer mechanism of human antimicrobial peptide LL-37

Aqeel Ahmad, M. Fawaz
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Abstract

Human antimicrobial peptides LL-37 have a variety of medicinal uses. It has been portrayed that this peptide has robust tumoricidal action in a range of malignancies, particularly ovarian cancer, lung cancer, breast cancer, prostate cancer, pancreatic cancer, malignant melanoma, and squamous cell carcinoma of the skin. It exhibits substantial anticancer action against a range of cancers, including colon cancer, gastric cancer, hematologic malignancy, and oral squamous cell carcinoma (OSCC), in comparison. In this review, we explored in depth the anticancer mechanism of action of LL-37 in numerous sorts of cancer. We have shown how LL-37 impedes colon cancer by eliciting caspase-independent apoptosis. LL-37, in addition, has been noticed to boost tumor-suppressive bone morphogenetic protein signaling in gastric cancer cells via restricting the proteasome, which has been previously reported. In this research, we investigated how DNA methylation interferes with the activity of the human CAMP (Cathelicidin antimicrobial peptide gene) promoter and, as a result, acts as a tumor inhibitor in mouth squamous cell carcinoma. Additionally, how LL-37 inhibits cancer cell development in hematologic malignancy has been explored through caspase-independent but Ca2+/calpain- and AIF-dependent processes.
人抗菌肽LL-37的抗癌机制
人抗菌肽LL-37具有多种药用价值。据报道,这种肽在一系列恶性肿瘤中具有强大的杀瘤作用,特别是卵巢癌、肺癌、乳腺癌、前列腺癌、胰腺癌、恶性黑色素瘤和皮肤鳞状细胞癌。相比之下,它对一系列癌症,包括结肠癌、胃癌、血液恶性肿瘤和口腔鳞状细胞癌(OSCC)显示出实质性的抗癌作用。本文就LL-37在多种肿瘤中的抗癌作用机制进行了深入探讨。我们已经展示了LL-37如何通过诱导caspase不依赖的细胞凋亡来阻止结肠癌。此外,已有报道发现LL-37通过限制蛋白酶体促进胃癌细胞中肿瘤抑制性骨形态发生蛋白信号传导。在这项研究中,我们研究了DNA甲基化如何干扰人类CAMP(抗菌肽基因)启动子的活性,从而在口腔鳞状细胞癌中发挥肿瘤抑制剂的作用。此外,LL-37如何抑制恶性血液病中的癌细胞发展已经通过caspase独立但Ca2+/calpain-和aif依赖的过程进行了探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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