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羟基酪醇[2-(3,4-二羟基苯基)-乙醇],一种存在于橄榄中的天然酚类化合物,可改变人 HepG2 肝癌细胞中的钙信号和活力。

Hydroxytyrosol [2-(3,4-dihydroxyphenyl)-ethanol], a natural phenolic compound found in the olive, alters Ca signaling and viability in human HepG2 hepatoma cells.

机构信息

Department of Medicine, Chang Bing Show Chwan Memorial Hospital, Changhua, Taiwan.

Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.

出版信息

Chin J Physiol. 2022 Jan-Feb;65(1):30-36. doi: 10.4103/cjp.cjp_74_21.

DOI:10.4103/cjp.cjp_74_21
PMID:35229750
Abstract

Hepatotoma is the leading type of primary liver cancer in adults and third cause of death in the world. Hydroxytyrosol is a natural phenol existing in olive (Olea europaea L.). Hydroxytyrosol is the chief ingredient of olive oil, which was early deemed to be the most robust antioxidant in olive oil. Hydroxytyrosol is known to inhibit various types of cancer by different methods. This study was aimed to delineate the action of hydroxytyrosol on viability and [Ca] in HepG2 hepatoma cells. Fura-2 was used to detect [Ca], and WST-1 assays were applied to explore cell cytotoxicity. Hydroxytyrosol elicited [Ca] raises. Eliminating external Ca diminished the Ca signal by 30%. Hydroxytyrosol-evoked Ca influx was diminished by 20% by three inhibitors of store-operated Ca channels and by a protein kinase C activator and an inhibitor. In the absence of Ca, thapsigargin eradicated hydroxytyrosol-provoked [Ca] raises. Suppression of phospholipase C (PLC) with U73122, a PLC inhibitor, did not inhibit hydroxytyrosol-elicited [Ca] raises. Hydroxytyrosol reduced cell viability. This cytotoxic action was not reversed by preincubation with BAPTA/AM, a cytosolic Ca binder. In sum, in HepG2 hepatoma cells, hydroxytyrosol elicited [Ca] raises by provoking PLC-unrelated discharge of Ca from ER and Ca influx through PKC-sensitive store-operated Ca entry. In addition, hydroxytyrosol elicited Ca-dissociated cytotoxicity.

摘要

肝细胞癌是成人原发性肝癌的主要类型,也是世界上第三大致死原因。羟基酪醇是一种存在于橄榄(Olea europaea L.)中的天然酚类物质。羟基酪醇是橄榄油的主要成分,早期被认为是橄榄油中最有效的抗氧化剂。羟基酪醇通过不同的方法被证实能抑制多种类型的癌症。本研究旨在描述羟基酪醇对 HepG2 肝癌细胞活力和[Ca]的作用。使用 Fura-2 检测[Ca],并应用 WST-1 测定法研究细胞毒性。羟基酪醇引起[Ca]升高。去除细胞外 Ca2+可使 Ca 信号降低 30%。三种钙库操纵性钙通道抑制剂、蛋白激酶 C 激活剂和抑制剂可使羟基酪醇诱导的 Ca2+内流减少 20%。在没有 Ca2+的情况下,毒胡萝卜素消除了羟基酪醇引起的[Ca]升高。用 PLC 抑制剂 U73122 抑制 PLC 并不能抑制羟基酪醇引起的[Ca]升高。羟基酪醇降低细胞活力。这种细胞毒性作用不能通过预先用细胞质 Ca 结合剂 BAPTA/AM 孵育来逆转。总之,在 HepG2 肝癌细胞中,羟基酪醇通过刺激 PLC 无关的内质网 Ca2+释放和通过 PKC 敏感的钙库操纵性钙内流引起[Ca]升高。此外,羟基酪醇还引起与 Ca2+相关的细胞毒性。

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