一种新的抗肺癌抗癌肽SSVAM-9的预测、设计、表征和评价

V. Palanimuthu
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引用次数: 0

摘要

一些抗癌药物正在被癌细胞抵抗,而化疗、放疗等治疗会产生严重的副作用。在免疫调节治疗中效率较低,CAR-T细胞、CAR-NK细胞需要较长时间才能在体外适应,长期使用可能引起癫痫发作、困局、脑震荡等。即使是CAR-T细胞和NK细胞的产生也是一个繁琐的过程。为了克服这种情况,可以使用抗癌肽,因为它们没有任何耐药性,而且它们可以非常有效,具有良好的细胞穿透性。这些多肽的优点是易于修饰、生产和配制。这次大流行向我们表明,鉴定和表征一种新型抗癌肽(ACP)是一个极其耗时和费力的过程。为了减少时间和劳动,本研究使用了几种计算机工具和算法,如SVM、RF、XGBoost和KNN来预测一种新的抗癌肽。经过多次研究,结合收集到的数据,预测了一种新的抗癌肽- SSVAM-9,它对肺癌有一定的抑制作用。其中,抗癌活性预测、细胞渗透预测均采用4种算法;在计算机模型中进行了稳定性预测、致敏性预测和肺癌预测活性预测。综合考虑各项参数,优选出一种较理想的新型ACP (SSVAM-9),由于该肽是一种稳定的肽,易于配制。该方法具有成本效益高、耗时短等优点,今后可在体内和体外进行研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predicting, designing, characterization and evaluation of a new novel anticancer peptide SSVAM-9 against the lung carcinoma, an insilico approach
Several anticancer drugs are getting resisted by the cancer cell and treatment like chemotherapy, radiation causes serious side effects. In immunomodulatory treatment the efficiency is less and CAR-T cells, CAR-NK cells require enormous time to get adopt to the in vitro and may cause seizures, dilemma, concussion in prolonged use against the cancer. Even the production of CAR-T cells and NK cells are tedious process. To overcome this situation, anticancer peptides can be used, as they don’t have any drug resistance and they can be highly potent, with good cell penetration. The advantages of these peptides are easy to modify, produce and formulate. This pandemic showed us that, identifying and characterizing a novel anticancer peptide (ACP) is an extremely time and labor consuming process. To reduce the time and labor, this study uses several in silico tools and algorithms like SVM, RF, XGBoost and KNN to predict a novel anticancer peptide. After several studies, with the collected data, a novel anticancer peptide – SSVAM-9 was predicted, which acts against the lung carcinoma. In this, anticancer activity prediction, cell permeation prediction with all 4 algorithms; stability prediction, allergenicity prediction and activity on lung carcinoma prediction were carried out in in silico model. Considering all the parameters, one best novel ACP was selected (SSVAM-9), and it can be easily formulated as the peptide is a stable one. This approach is an advantageous one as it is cost efficient and less-time consuming which can be studied in vivo and in vitro in future.
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