Determination of the anticancer activity of standardized extract of Centella asiatica (ECa 233) on cell growth and metastatic behavior in oral cancer cells.

IF 2.1 Q3 CHEMISTRY, MEDICINAL Research in Pharmaceutical Sciences Pub Date : 2024-04-01 DOI:10.4103/RPS.RPS_81_23
Suwisit Manmuan, Sukannika Tubtimsri, Nattaya Chaothanaphat, Nipatha Issaro, Mayuree H Tantisira, Ponwit Manmuan
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Abstract

Background and purpose: The anticancer drugs used for oral cancer treatment present many disadvantages, such as low solubility, low permeability, and poor bioavailability. However, the anticancer activity of ECa 233 has not been widely studied. Therefore, the anticancer activity of ECa 233 was investigated in this study.

Experimental approach: MTT assay was carried out to determine cell viability. Characterizations of cell apoptosis were monitored using DAPI and FDA staining and Hoechst 33258 and AO staining. Confirmation of the apoptosis-induced KON cells was done using annexin V-FITC staining, and ROS generation was determined by DCFDA staining. Cell death and the cell cycle arrest activity of ECa 233 were demonstrated by a flow cytometer. The anti-migration and anti-invasion properties of ECa 233 were examined. The anti-proliferative of ECa 233 was investigated. Cellular uptake of ECa 233 was measured by TEER values. The pharmacokinetics of ECa 233 were estimated using the pkCSM web server.

Findings/results: ECa 233 decreased the KON cell viability. Morphological analysis showed the KON cells' loss of cell stability and structure, disorganized nucleus and cytoplasm, and induced cell death. ECa 233 acted as a cell cycle arrest in the G0/G1 phase and reduced the migration and invasion ability in KON cells. TEER values significantly increased in KON cells, which decreased cell colony and multicellular spheroid formations. The pharmacokinetic profiles of the main components are of interest for future usage.

Conclusion and implication: ECa 233 can be used as an alternative therapy as well as a medicinal plant selected for sensitizing oral cancer cells to chemotherapy.

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确定积雪草标准化提取物(ECa 233)对口腔癌细胞生长和转移行为的抗癌活性。
背景和目的:用于口腔癌治疗的抗癌药物存在许多缺点,如溶解度低、渗透性低和生物利用度差。然而,ECa 233 的抗癌活性尚未得到广泛研究。因此,本研究对 ECa 233 的抗癌活性进行了研究:实验方法:采用 MTT 法测定细胞活力。使用 DAPI 和 FDA 染色以及 Hoechst 33258 和 AO 染色监测细胞凋亡的特征。用附件素 V-FITC 染色法确认凋亡诱导的 KON 细胞,用 DCFDA 染色法测定 ROS 生成。ECa 233 的细胞死亡和细胞周期停滞活性由流式细胞仪进行了证明。研究还考察了 ECa 233 的抗迁移和抗侵袭特性。研究了 ECa 233 的抗增殖性。通过 TEER 值测量了细胞对 ECa 233 的吸收。使用 pkCSM 网络服务器估算了 ECa 233 的药代动力学:ECa 233降低了KON细胞的活力。形态学分析表明,KON细胞丧失了细胞稳定性和结构,细胞核和细胞质紊乱,并诱导细胞死亡。ECa 233能使细胞周期停滞在G0/G1期,并降低KON细胞的迁移和侵袭能力。KON细胞的TEER值明显增加,细胞集落和多细胞球形形成减少。主要成分的药代动力学特征对今后的应用具有重要意义:ECa 233 可作为一种替代疗法,也可作为一种药用植物,用于提高口腔癌细胞对化疗的敏感性。
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来源期刊
Research in Pharmaceutical Sciences
Research in Pharmaceutical Sciences CHEMISTRY, MEDICINAL-
CiteScore
3.60
自引率
19.00%
发文量
50
审稿时长
34 weeks
期刊介绍: Research in Pharmaceutical Sciences (RPS) is included in Thomson Reuters ESCI Web of Science (searchable at WoS master journal list), indexed with PubMed and PubMed Central and abstracted in the Elsevier Bibliographic Databases. Databases include Scopus, EMBASE, EMCare, EMBiology and Elsevier BIOBASE. It is also indexed in several specialized databases including Scientific Information Database (SID), Google Scholar, Iran Medex, Magiran, Index Copernicus (IC) and Islamic World Science Citation Center (ISC).
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