PO.MCB02.01 · 分子与细胞生物学

Leptospermum petersonii甲醇和乙酸乙酯粗提物对胰腺癌和前列腺癌细胞的抗转移及促凋亡作用

Leptospermum petersonii methanol and ethyl acetate crude extracts as antimetastatic and apoptotic effects against pancreatic and prostate cancer cells

编号 4654 展板 3 时间 4/21 09:00–12:00 区域 Section 20 主讲 Lesetja Motadi, PhD
分会场 Cell Death Regulation and Therapeutic Resistance in Cancer
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作者与单位 Authors & Affiliations

Lesetja Motadi1, Maria Matlou2

1University of Johannesburg, Johannesburg, South Africa,2Biochemistry, University of Johannesburg, Johannesburg, South Africa

摘要 Abstract

中文摘要
癌症仍是全球头号医疗保健挑战,据估计每9人中就有1人在其一生中罹患癌症。随着癌症日益普遍,研究聚焦于寻找可能改变癌症治疗的姑息护理和天然疗法。本项目旨在研究药用植物Leptospermum petersonii活性化合物对胰腺癌和前列腺癌细胞的抗癌和抗转移作用。采用了以下技术:TLC、柱层析和NMR色谱、alamarBlue法、ATP法、划痕愈合实验、Hoechst染色、caspase检测、琼脂糖凝胶(DNA片段化分析)和RT-PCR。通过细胞活力检测,识别出甲醇粗提物的IC₅₀约为100 µg/mL,其对MIA PaCa-2细胞的细胞毒作用大于对PC3细胞。EtOAc提取物的细胞毒指数IC₅₀ > 100 µg/mL,表明即使在100 µg/mL剂量下仍有60%的细胞存活,因此由于其效力不足而终止了后续测试。Caspase 3/7检测和DNA片段化显示出一些支持凋亡的阳性结果。划痕愈合实验表明未处理细胞在24小时内愈合缺口,而处理细胞愈合所需时间更长。基因表达显示RB1和checkpoint 1上调,二者对DNA损伤和凋亡诱导是必需的。总之,结果提示L. petersonii提取物中可能存在可用于开发抗癌药物的化合物。
查看英文原文 English abstract
Cancer remains number one health care challenge worldwide with an estimation of 1 in 9 people developing cancer in their lifetime. As cancer becomes increasingly prevalent, research focuses on finding palliative care and natural treatments that could transform cancer therapeutics. The aim of the project was to investigate the anti-cancer and anti-metastatic effects of medicinal plant Leptospermum petersonii 's active compounds against pancreatic and prostate cancer cells. The following techniques were employed: TLC, Column and NMR chromatography, alamarblue assay, ATP assay, wound healing assay, Hoechst Staining, caspase assay, Agarose gel (DNA fragmentation analysis) and RT-PCR. Through cell viability assay and IC₅₀ of approximately 100 µg/mL for the methanolic crude extract was identified with greater cytotoxic effect on MIA PaCa-2 than PC3 cells. The EtOAc extract showed cytotoxicity indices IC₅₀ > 100 µg/mL signifying 60% of the cells were viable even at a dose of 100 µg/mL and thus led to the termination of additional testing because of its ineffective potency. Caspase 3/7 assay and DNA fragmentation had shown some positive result in support of apoptosis. Wound healing demonstrated untreated cells healed the gap in 24 hours, whereas treated cells took longer to do so. Gene expression showed upregulation of RB1 and checkpoint 1 which are necessary for DNA damage and apoptosis induction. In conclusion, the results suggest that there might be compounds within L. petersonii extracts that can be exploited for anticancer agent.
利益披露 Disclosure
L. Motadi, None.. M. Matlou, None.

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