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石斛属植物抗肿瘤活性成分及其机制研究进展

2021-01-12李健王美娜赵美丽李鹤娟胡玥陈建兵

广西植物 2021年10期
关键词:活性成分抗肿瘤石斛

李健 王美娜 赵美丽 李鹤娟 胡玥 陈建兵

摘 要:石斛属(Dendrobium)是兰科植物中的第二大属,很多石斛属植物是传统的名贵药用植物,具有良好的抗肿瘤作用。近年来石斛属植物抗肿瘤研究取得了显著进展,该文对石斛属植物的抗肿瘤主要活性成分、提取方法以及抗肿瘤机制等方面进行了归纳。石斛属植物抗肿瘤主要活性成分有多糖、生物碱、菲类、联苄类、芴酮类化合物等,抗肿瘤作用机制主要有增强机体免疫力、抑制癌细胞增殖、促进癌细胞凋亡、调控或阻滞癌细胞周期、抗氧化和清除自由基、改变信号通路传导等。在此基础上,进一步提出加强对石斛属植物抗癌方面的深入研究,挖掘更多的石斛属药用资源及其特征成分,深入解析它们的抗肿瘤作用机制,建立全面的评价体系,为开发石斛属植物抗癌药物提供理论基础,为合理、有效地利用石斛属资源提供科学依据。

关键词:石斛,抗肿瘤,活性成分,作用机制

中图分类号:Q946

文献标识码:A

文章编号:1000-3142(2021)10-1730-16

Abstract:Dendrobium is the second largest genus of Orchidaceae. Many species of Dendrobium are traditional valuable medicinal plants and have pharmacological activities in antitumor. In recent years,remarkable progress has been made in the antitumor researches of Dendrobium species. The main antitumor ingredients,extraction methods and antitumor mechanisms of Dendrobium species were summarized in this paper. The main antitumor active ingredients of Dendrobium are polysaccharides,alkaloids,phenanthrenes,benzyls and fluorenones. The antitumor mechanisms of Dendrobium species mainly include enhancing body immunity,inhibiting proliferation of cancer cells,promoting apoptosis of cancer cells,regulating or blocking cancer cell cycle,antioxidation and scavenging free radicals,and changing signal pathway conduction. Based on previous researches,we further proposed that much more effort are needed on the antitumor researches of Dendrobium species. For example,exploring more antitumor Dendrobium resources and their characteristic ingredients,analyzing their antitumor mechanism,and establishing comprehensive evaluation system. This article could provide experimental and theoretical foundations for developing new antitumor medicine from Dendrobium species,and provide scientific basis for the rational and effective utilizatin of Dendrobium resources.

Key words:Dendrobium,antitumor,active ingredient,mechanism of action

石斛屬(Dendrobium)是兰科(Orchidaceae)植物中的第二大属,种类繁多,常附生于海拔较高的林中树干或湿润岩石上,喜半荫环境,广泛分布于亚洲、澳大利亚、欧洲等地(Chen et al.,2009)。Flora of China记载我国石斛属有78种,主要分布于云南、贵州、广西、广东、海南和台湾等地(Chen et al.,2009)。中医药著作记载石斛具有生津益胃、益精强阴等药理作用(国家中医药管理局,1999)。近年来,石斛属植物的药用价值,特别是其在抗肿瘤活性方面的作用逐渐受到国内外研究者的重视。研究发现,多种石斛属植物具有显著的抗肿瘤作用,如铁皮石斛(D. catenatum)可抑制小鼠Lewis肺癌肿瘤细胞、人肝癌细胞HepG2、人肺癌细胞A549、人畸胎瘤干细胞NCCIT及小鼠畸胎瘤干细胞F9的生长,诱导HepG2癌细胞凋亡(刘亚娟等,2014;王杰等,2014;Xing et al.,2018b; 罗颖懿等,2019);金钗石斛(D. nobile)可抑制结肠腺癌细胞Caco-2、人三阴性乳腺癌细胞的增殖等(王亚芸,2015;宋林霞,2019)。本文对石斛属植物主要抗肿瘤活性成分、提取方法、抗肿瘤机制等研究进展进行了综述,以期为深入研究和应用石斛属植物抗肿瘤作用提供参考。

1 主要抗肿瘤活性成分及作用

石斛属植物的主要化学成分有多糖、生物碱、菲类、联苄类、芴酮类、黄酮类、木脂素类、香豆素类、蒽醌类、苷类、酯类等化合物(王东晖等,2019)。研究表明,石斛属植物抗肿瘤作用活性成分主要有生物碱类、多糖类、酚类等(王琳炜,2017;周威等,2018;宋林霞,2019),详见表1。

1.1 多糖

多糖是石斛属植物最主要的活性成分,具有抗炎、抗氧化、抗病毒、抗肿瘤、提高免疫力等功效(Xing et al.,2013),主要由葡萄糖、半乳糖、木糖及阿拉伯糖和甘露糖组成(周思静等,2018)。石斛多糖对肉瘤180肿瘤细胞(Wang et al.,2010)、H22肝癌腹水细胞(何铁光等,2007)、HepG2人肝癌细(Xing et al.,2018b)、人肺癌细胞A549(刘亚娟等,2014)、人畸胎瘤干细胞NCCIT(刘亚娟等,2014)等肿瘤细胞均具有良好的抑制作用。铁皮石斛多糖在体外联合白细胞介素-2能显著增强脐带血及恶性肿瘤病人外周血LAK细胞杀伤肿瘤细胞的作用(罗慧玲等,2000)。Tong et al.(2016)研究了齿瓣石斛(D. devonianum)茎中水溶性多糖对S180荷瘤小鼠的抗肿瘤活性和免疫刺激作用,结果表明水溶性多糖可通过改善特异性和非特异性免疫应答以及增加结肠总短链脂肪酸SCFAs的浓度,显著抑制S180荷瘤小鼠中移植肿瘤的生长。罗傲雪等(2007)研究了叠鞘石斛(D. denneanum)不同浓度的多糖、醇提物及水提物对人肝癌细胞SMMC-7721生长的抑制作用,结果表明多糖对癌细胞抑制作用最强,是叠鞘石斛抗肿瘤最为有效的成分。Liu et al.(2019)综述了近年来有关天然多糖抗肿瘤活性的研究进展,认为多糖具有一定的抗肿瘤活性与改善肠道渗漏、避免营养不良、增强免疫稳态有关。Deng et al.(2018)通过研究石斛多糖的结构、化学性质和免疫调节活性,发现石斛多糖可以提高包括NO释放和吞噬在内的巨噬细胞的免疫功能,可以作为一种天然的免疫刺激剂。Liu et al.(2019)研究表明石斛多糖有利于免疫抑制条件下的小鼠提高巨噬细胞的生存能力和吞噬能力。球花石斛(D. thyrsiflorum)多糖可显著增加脾脏重量、增强巨噬细胞的吞噬功能、加速碳粒的清除以及刺激B淋巴细胞的增殖,是良好的免疫调节剂(宋宁等,2006)。黄花石斛(D. tosaense)多糖可显著增加脾脏自然杀伤的细胞数量和细胞毒性,增强巨噬细胞吞噬作用,诱导脾细胞中IL-2细胞因子和IFN-SymbolgA@

细胞因子的产生,发挥着强大的免疫调节剂的作用(Yang et al.,2014)。因此,石斛多糖具有抗肿瘤活性的机制可能与石斛多糖具有免疫调节活性密切相关。

1.2 生物碱

石斛属植物中已发现52个生物碱成分,常见含有生物碱的有7种,即金钗石斛、束花石斛(D. chrysanthum)、玫瑰石斛(D. crepidatum)、棒节石斛(D. findleyanum)、铬黄石斛(D. friedericksianum)、报春石斛(D. primulinum)和黄喉石斛(D. signatum)(李振坚等,2019)。1932年,铃木秀干首次从金钗石斛中提取到石斛碱,是石斛属植物中最早发现的化合物(徐琼等,2010)。石斛生物碱的药理作用主要表现在清热解毒、抗肿瘤、降血糖血脂、抗血栓、改善脑供血等方面(何沁嶷,2016;张明辉,2016)。石斛生物碱对多种癌细胞具有抑制作用,如乳腺癌、结肠癌、Lewis肺癌等。安欣等(2015)研究发现,石斛生物碱可以通过调控乳腺癌细胞MCF-7的细胞周期来诱导细胞凋亡。和磊等(2017)发现,石斛脂溶性生物碱提取物可以诱导上调促细胞凋亡因子,并通过线粒体凋亡途径使释放到胞浆中的凋亡因子与关键蛋白Caspase-9酶结合,触发细胞凋亡过程,最终引起人结肠癌HT-29细胞凋亡。王杰等(2014)通过研究鲜铁皮石斛提取物的抗Lewis肺癌机制以及对Lewis肺癌小鼠瘤块血管内皮生长因子VEGF、增殖细胞核抗原PCNA、肿瘤组织微血管密度MVD的影响,发现鲜铁皮石斛生物碱可抑制小鼠Lewis肺癌肿瘤细胞的生长。其机制可能是通過促进T细胞亚群的生长,与淋巴细胞膜上的T细胞生长因子受体结合,从而调节机体的细胞免疫发挥抗肿瘤作用;也可能是通过鲜铁皮石斛生物碱和多糖联合抑制瘤块VEGF、PCNA、MVD的表达来实现。金钗石斛的水溶性生物碱可通过诱导细胞G1期阻滞,从而抑制结肠腺癌细胞Caco-2的生长,其水溶性生物碱和脂溶性生物碱粗提物都可激活Caspase-3酶,诱导癌细胞凋亡,抑制结肠腺癌细胞Caco-2的增殖(王亚芸,2015)。宋林霞(2019)研究了金钗石斛生物碱对三阴性乳腺癌细胞的作用及机制,发现金钗石斛生物碱对人三阴性乳腺癌细胞增殖具有明显的抑制作用。

1.3 酚类化合物

石斛属植物中的酚类化合物主要包括菲类、联苄类、芴酮类等,具有抗肿瘤、降血糖、提高免疫力等功效(周婧等,2010;Zhu et al.,2019)。石斛酚具有抑制非小细胞肺癌H460细胞上皮间质转化的能力(Unahabhokha et al.,2016a),可抑制H460细胞的迁移(Charoenrungruang et al.,2014),抑制肝癌细胞HepG2的生长及诱导HepG2细胞的凋亡(陈欢欢,2017)、抑制乳腺癌细胞的活力和迁移(Yu et al.,2018)。长苏石斛(D. brymerianum)全株甲醇提取物分离的8种酚类化合物中,杓唇石斛素、石斛酚、lusianthridin和dendroflorin对人类H460肺癌细胞具有明显的细胞毒性,表现出一定的抗肿瘤活性(Pornprom et al.,2015)。鼓槌石斛(D. chrysotoxum)中含有的鼓槌菲对艾氏腹水癌的抑瘤率可达到62.25%(马国祥等,1994)。联苄类化合物具有抗氧化、抗癌等活性(Hu et al.,2008),目前关于石斛成分研究较多的毛兰素即属于联苄类化合物。毛兰素可诱导膀胱癌细胞(朱启彧,2013;Zhu et al.,2019)、鼻咽癌细胞(Liu et al.,2019)、结肠癌SW480细胞(崔旭琴等,2011)、结肠癌细胞Caco-2(崔名扬等,2016)、胃癌细胞SGC-7901(洪卫等,2008)、乳腺癌T47D细胞(Sun et al.,2016a)的凋亡,能显著抑制人肝癌Huh7细胞和HepG2细胞的增殖(苏鹏等,2011;王晶,2013)。石斛菲醌是从石斛属中分离出的联苄类化合物。石斛菲醌可诱导人类结肠癌HCT-116细胞、肺癌A549细胞显示出典型的凋亡特征(Chen et al.,2008; Kuo et al.,2008),通过抑制Rac1蛋白活性来抑制前列腺癌的迁移(Lu et al.,2014),通过上调卵巢癌增生及转移相关基因CASP3、CASP9、CAV1及下调SOX2基因的表达来抑制人卵巢癌细胞HO-8910PM的增殖和转移(张晓文等,2016)。从密花石斛(D. densiflorum)中提取的菲醌物质杓兰素具有抗肿瘤迁移等多种药理活性特性。Treesuwan et al.(2018)使用H460和H23细胞作为体外模型研究了杓兰素对肺癌细胞的抗转移潜力,结果表明杓兰素通过抑制Akt/GSK-3β信号传导减少非小细胞肺癌细胞的上皮间质转化,对抑制肺癌转移具有良好的药理作用。此外,一项关于杓兰素使非小细胞肺癌H460细胞对顺铂介导的细胞敏感凋亡的研究表明,杓兰素能够激活caspase-3并下调抗凋亡蛋白Bcl-2和Bcl-xL的表达,诱导人肺癌H460细胞凋亡并增强顺铂介导的癌细胞凋亡,杓兰素作为抗癌药或与顺铂结合使用可能会增加肺癌治疗的成功率(Wattanathamsan et al.,2018)。

2 主要抗肿瘤活性成分提取方法

石斛属植物主要活性成分提取方法有水提取(刘奇等,2019)、醇提取(黄丽等,2017)、水提醇沉(贺雨馨等,2018)、超临界流体萃取(马成林,2014)、微波提取(柴连周等,2018)、超声提取(郭旭等,2019)、酶提法(敖娇等,2018)、闪式提取(蔡兴等,2016)、半仿生提取(戴玮等,2018)等,各提取方法的最佳工艺参数,一般需要通过对各项影响实验结果的单因素进行考察实验,结合正交优化实验研究最终确定。

2.1 水提法

水提法是最经典常用的提取方法,提取容液的料液比、浸提温度、提取时间以及提取次数都是影响水提效果较多的单因素。刘奇等(2019)以铁皮石斛多糖提取率、固含量为考察指标,提出铁皮石斛水提最佳工艺条件为料液比1∶30、提取3次、每次提取5 h。王丽霞等(2019)采用正交试验方法,发现在料液比1∶80、提取温度80 ℃、提取3次、每次提取2 h的工艺条件下铁皮石斛多糖提取效率最高。单冰冰等(2017)研究表明,铁皮石斛多糖最优提取工艺为料液比1∶70、提取温度90 ℃、提取2次、每次提取78.5 min。王洪云等(2017)通过正交试验对齿瓣石斛多糖提取的研究发现,最优工艺为料液比1∶25、温度100 ℃、提取次数2次、每次提取1 h。水提法操作简单,提取温度高、提取次数多则提取效率高。因此,水提法能耗较高,成本相比于其他提取工艺也高。

2.2 酶提取

酶提取效率较高,近年来应用较广泛(敖娇等,2018)。酶的种类、添加量、酶解温度、酶解时间、料液比、pH值等因素均会影响提取效率。杨岩等(2017)使用α-L-鼠李糖苷酶提取铁皮石斛多糖,在加酶量为2.5%、酶解温度为40 ℃、酶解时间为1 h时提取效率最高。韩冉等(2017)对铁皮石斛多糖提取工艺优化及分子量分析结果表明,果胶酶浓度1 500 U·L-1、酶解pH值6.0、酶解温度60 ℃为最优提取工艺参数。敖娇等(2018)对金钗石斛中生物碱与多糖联合酶提工艺的优化结果表明,木瓜蛋白酶提取的最佳条件为加酶量0.10 g,料液比1∶50,酶解温度45 ℃,酶解时间2 h;纤维素酶提取的最佳条件为加酶量0.30 g,料液比1∶40,酶解温度50 ℃,酶解时间2 h;果胶酶提取的最佳条件为加酶量0.45 g,料液比1∶40,酶解时间2 h。虽然酶提取具有高生产率、能耗低、污染少等优点,但酶反应控制条件要求高,酶解温度、酶解时间、酶用量都影响提取效率,不易操作。

2.3 超声提取

超声提取操作简单,短时间内可达到较高的提取效率,常用来结合其他提取工艺技术,具有提取时间短、能耗低、提取效率高等优点。超声功率、超声时间、提取温度、料液比参数等因素均会影响提取率。郭旭等(2019)超声结合60%甲醇提取河南石斛(D. henanense)游离氨基酸的最优工艺条件为料液比1∶40、超声时间30 min、超声功率240 W、提取4次。杨晓娜等(2018)对铁皮石斛花色苷的超声波结合60%的酸性乙醇提取工艺及抗氧化活性的研究表明,花色苷提取最优工艺参数为乙醇体积分数30%、料液比1∶20、超声温度40 ℃、超声时间70 min、超声波功率180 W。邱现创等(2018)研究表明,在料液比1∶50.26、温度41.74 ℃、超声时间28.65 min的条件下,铁皮石斛多糖的提取效率最高。魏明等(2016)研究表明,超声波结合纤维素酶法提取霍山石斛(D. huoshanense)多酚最优工艺参数为酶质量浓度2.1 mg·mL-1、酶解温度57 ℃、酶解时间71 min、酶解pH值5、超聲功率180 W、超声时间20 min。余芳等(2016)研究发现,料液比1∶25、超声时间40 min、水提时间120 min、水提温度80 ℃为超声提取金钗石斛多糖的最优工艺参数。

2.4 微波提取

微波技术具有反应时间短、可进行选择性加热、节能环保、操作简单、反应效率高等优点,较传统水提法工艺在中药天然活性成分提取上的效果良好且应用广泛(柴连周等,2018)。微波功率、微波时间、料液比等提取工艺参数都是影响提取效率的因素。缪园欣等(2019)对铁皮石斛花多糖提取工艺及体外抗氧化性研究表明,在料液比1∶50、微波时间3 min、超声时间55 min、微波功率450 W的条件下,铁皮石斛花多糖超声波—微波协同提取效率最高。陈盛余等(2017)将微波技术应用于铁皮石斛多糖的提取,得到的最佳工艺条件为料液比1∶45、提取温度95 ℃、提取时间30 min、微波功率900 W。

在石斛抗肿瘤活性成分研究中,能否高效提取其活性成分是研究石斛抗肿瘤作用的关键,不同提取方法对石斛有效成分抗肿瘤活性的影响较为显著。张雪琴等(2019)研究发现叠鞘石斛乙醚提取物相比醇或水提取物对肺癌细胞具有更强的抑制作用。李莹等(2018)研究了金钗石斛与叠鞘石斛不同极性成分的提取及其对肺癌A549细胞的抑制作用,发现石斛乙醚提取物对肺癌细胞的抑制作用较强,水和乙醇提取法对石斛抗肿瘤成分的提取效率较低。利用水提乙醇沉淀法从铁皮石斛茎中提取纯化后的多糖组分均具有高效的抗氧化和抗肿瘤活性(Xing et al.,2018b)。鲍丽娟(2007)研究了霍山石斛、铁皮石斛、金钗石斛和马鞭石斛(D. fimhriatum)的水提物、石油醚、乙酸乙酯及正丁醇提取部位,发现不同极性部位提取物对人宫颈癌HelsS3和肝癌HepG2细胞株抑制作用程度不同。严慕贤等(2015)研究了金钗石斛水溶性多糖与碱溶性多糖对人宫颈癌HeLa细胞增殖的影响,发现水溶性多糖质量浓度较高时,对人宫颈癌HeLa细胞的生长有抑制作用,此作用随着质量浓度的增高而增强,而碱溶性多糖则与之相反。综上所述,对石斛活性成分的提取,同一提取方法的最佳工艺条件并不相同,不同工艺的适用范围尚未得到深入研究,但成分提取最佳方案的探索基本遵循了首先确定影响因素,然后进行单因素实验和正交实验研究,最终确定最佳工艺参数的规律。

3 抗肿瘤机制研究

3.1 增强机体免疫力

免疫系统在人体抵抗癌症的天然防御中占有重要地位,免疫系统可以消除或抑制病毒感染,从而保护宿主免受病毒诱导的肿瘤侵袭;可以及时清除病原体并迅速消炎,阻止有利于肿瘤发生的炎性环境建立;可以根据肿瘤特异性抗原或细胞应激诱导的分子表达,特异性识别和消除肿瘤细胞(Swann & Smyth,2007)。叠鞘石斛多糖可通过增强机体的抗氧化能力提高抗肿瘤的免疫功能(罗傲雪等,2007)。Yang et al.(2017)的免疫药理研究表明,自D. Taiseed Tosnobile中分离的多糖(DTTPS)可增加脾自然杀伤NK细胞的数量和毒性,增强巨噬细胞吞噬作用,诱导IL-2细胞因子和IFN-SymbolgA@

细胞因子产生,DTTPS被认为是有效的免疫调节剂。Huang et al.(2015)使用环磷酰胺诱导的免疫抑制小鼠模型,重点研究了铁皮石斛栽培种的茎及其两个多糖组分(粗多糖和纯化多糖)的免疫调节功能,结果表明铁皮石斛栽培种的免疫调节活性和野生种相同,纯化后的多糖是铁皮石斛中关键的生物活性成分之一,其主要结构为O-乙酰-葡甘露聚糖,β-(1→4)糖苷键和O-乙酰基结构可能是负责免疫调节活动的功能结构。He et al.(2016)进一步证实纯化的结构为O-乙酰-葡甘露聚糖的铁皮石斛多糖具有显著的免疫调节活性,其免疫机制是通过上调NF-кB和ERK1/2信号通路来实现。Huang et al.(2018)从铁皮石斛茎中分离得到的2,3-O-乙酰化的1,4-β-d-葡甘露聚糖可通过TLR4信号通路介导的NF-кB诱导免疫反应,调节免疫反应、增强免疫力。Liang et al.(2019)研究证明铁皮石斛多糖可增强结直肠癌小鼠肿瘤微环境中细胞毒性T淋巴细胞CTLs的代谢功能,减少CTLs中线粒体的损失,并抑制CTLs中免疫抑制因子PD-1的表达,恢复肠屏障功能,增强肠道抗肿瘤免疫反应,抑制结直肠癌。综上所述,石斛可以作为免疫调节剂,增强机体免疫力,提高机体抗肿瘤能力。

3.2 抑制癌细胞增殖

抑制癌细胞增殖可保护宿主免受癌症进一步扩大化的影响。多种石斛提取物具有抑制癌细胞增殖的作用。鼓槌石斛中提取的天然产物毛兰素可通过减少Bcl-2的表达,激活Caspase信号传导,诱导人乳腺癌细胞株T47D细胞凋亡,进而有效抑制T47D细胞的增殖。毛兰素能抑制细胞周期蛋白依赖性激酶的表达并引起细胞周期停滞,通过调节基质金属蛋白酶MPP及其组织特异性抑制物TIMP的稳态表达来实现抑制T47D细胞的迁移,同时不会影响正常乳腺上皮细胞系MCF10A的增殖(Sun et al.,2016a)。不同生长年限的铁皮石斛醇提取物对人肝癌细胞HepG2、人宫颈癌细胞HeLa均有抗增殖作用,生长期限较长的,其抗HeLa肿瘤活性作用也较强(林丽珍等,2018)。铁皮石斛茎乙醇提取物具有抑制人鼻咽癌CNE1和CNE2细胞增殖的作用(邓鹏,2010)。叠鞘石斛乙醚提取物可干扰癌细胞内蛋白等物质的代谢过程,干扰癌细胞正常的黏附功能以及细胞周期调控,使癌细胞的自我修复机制出现异常,导致癌细胞的黏附与增殖功能受损,从而抑制肺癌细胞A549的增殖(张雪琴等,2019)。叠鞘石斛的黄酮类化合物可通过诱导人肝癌细胞HepG2显著凋亡来抑制HepG2细胞的增殖(Zhou et al.,2018)。细胞周期蛋白依赖性激酶通过维持细胞周期在控制细胞增殖中起关键作用(张京玉等,2015),有效活性成分通过抑制细胞周期蛋白依赖性激酶的表达量可抑制癌细胞增殖。对Huh7癌细胞的增殖抑制作用中,毛兰素通过抑制Akt激酶活性、下调Mcl-1蛋白表达活性以及激活PARP活性的方式来实现(苏鹏等,2011)。

3.3 促进癌细胞凋亡

抗肿瘤治疗的障碍主要是恶性肿瘤细胞的抗凋亡能力,癌细胞对凋亡敏感的识别策略是抗肿瘤研究的首要任务(Magwere,2009)。叠鞘石斛中的杓唇石斛素可增加活性氧ROS的生成,调节Bax/Bcl2(促凋亡蛋白/抗凋亡蛋白)比值,进而诱导胰腺癌细胞凋亡(Zhang et al.,2017)。鐵皮石斛多糖可通过诱导Bcl-2的下调及Bax的上调,改变线粒体的功能、ROS的产生及与凋亡相关蛋白表达来诱导人肝癌细胞HepG2的凋亡(Xing et al.,2018b)。在1-甲基-3-硝基-1-亚硝基胍MNNG诱导的大鼠胃肿瘤发生过程中,铁皮石斛水提取物可下调MDA和8-羟基-脱氧鸟苷8-OHdG的表达,上调GSH-PX和IL-2的活性,表明铁皮石斛具有抗氧化作用,可调节肿瘤发生相关的细胞因子,诱导癌细胞凋亡,从而达到预防胃癌的目的(Zhao et al.,2016)。毛兰素通过线粒体膜的改变、死亡受体的激活和caspase-3、-8、-9的激活,引起鼻咽癌细胞系(NPC-039和NPC-BM)的凋亡和阻滞细胞周期,使用毛兰素及其抑制剂可以增加癌细胞凋亡的发生率(Liu et al.,2019)。在D. venustum中分离得到的Phoyunnanin E通过活化caspase-3、-9和聚合酶的裂解,使细胞核浓缩和碎片化,可显著诱导H460肺癌细胞凋亡;Phoyunnanin E可通过增加细胞内p53蛋白的积累,利用p53蛋白依赖途径介导细胞凋亡;Phoyunnanin E可诱导H23肺癌细胞的凋亡(Phiboonchaiyanan et al.,2018)。

3.4 调控或阻滞细胞周期

细胞周期内G1到S和G2到M两个阶段处于复杂活跃的分子水平变化的时期,容易受环境条件的影响。因此,阻滞和调控G1/S期、G2/M期对促进癌细胞凋亡有重要意义。毛兰素可通过诱导骨肉瘤、膀胱癌的细胞周期G2/M期阻滞、凋亡和自噬显示出抗肿瘤活性(Wang et al.,2016; Zhu et al.,2019)。细茎石斛(D. moniliforme)可通过诱导细胞在G2/M期的周期阻滞和调控乳腺癌细胞中的关键生物标志物来降低人乳腺癌细胞株MCF-7细胞的生存能力(Sun et al.,2016b)。金钗石斛的菲类衍生物3,4-二甲氧基-2,7-菲二醇Nudol是细胞周期蛋白依赖性激酶的良好抑制剂,Nudol通过引起骨肉瘤细胞U2OS中G2/M期的细胞周期停滞,对骨肉瘤细胞具有抗增殖活性(Zhang et al.,2019)。束花石斛乙醇提取物可通过上调人体抑癌基因p53干扰宫颈癌HeLa细胞周期进程并导致S期细胞的延迟,进而诱导HeLa细胞的凋亡(Prasad et al.,2017)。D. formosum乙醇提取物通过对Dalton淋巴瘤在细胞周期G2/M期的阻滞,可促进Dalton淋巴瘤细胞的明显凋亡,显著增加Dalton淋巴瘤小鼠的生存时间(Prasad & Koch,2014)。

3.5 抗氧化和清除自由基

癌症的发生与发展与自由基过剩密切相关(Stohs,1995),抗氧化和清除自由基对于癌症防治具有重要意义。铁皮石斛多糖能抑制8-羟基-脱氧鸟苷8-OHdG的活性,并激活核因子红细胞2相关因子NRF2途径及其相关的抗氧化酶HO-1和氧化还原酶NQO-1的表达,改善抗氧化活性并保护胃粘膜细胞免受氧化损伤,防止1-甲基-3-硝基-1-亚硝基胍MNNG诱导的胃癌癌前病变以及随后的肝肾损害(Zhao et al.,2019b)。铁皮石斛多糖可显著调节胃癌癌前病变大鼠模型中的9种内源性代谢产物,其中最重要的一种是甜菜碱,它具有很强的抗氧化活性,从而具有一定的抗肿瘤作用(Zhao et al.,2019a)。Paudel et al.(2019)对玫瑰石斛茎的乙醇和丙酮提取物的抗氧化性和对癌细胞细胞毒性的研究发现,这两种提取物在浓度分别为73.90和99.44 μg·mL-1时显示出对DPPH自由基(IC50)的抑制作用,在浓度为800 μg·mL-1的条件下,氯仿提取物抑制人宫颈癌HeLa细胞生长的 81.49%±0.43%,己烷提取物抑制人胶质母细胞瘤U251细胞生长的76.45%±4.26%,说明玫瑰石斛乙醇和丙酮提取物具有抗氧化性和癌细胞毒性。

3.6 抑制信号通路表达

抑制或改变细胞信号通路的表达,可以增强机体免疫力、诱导癌细胞的凋亡、抑制癌细胞增殖和迁移。铁皮石斛多糖的免疫机制通过上调NF-кB和ERK1/2信号通路来实现(He et al.,2016)。在抑制HepG2肝癌细胞增殖中,毛兰素诱导的细胞凋亡过程有抑制Akt激酶活性、抑制JAK/STAT3信号通路、抑制Wnt信号通路及TGF-B3l信号通路等多条分子细胞信号通路参与(苏鹏等,2011)。在促进人宫颈癌细胞HeLa凋亡过程中,毛兰素通过调节ERK1/2信号通路和线粒体凋亡通路来抑制细胞增殖,促进细胞凋亡(Li et al.,2018)。Yu et al.(2018)研究发现,石斛酚不同剂量处理可降低HEK293细胞中磷酸化LRP6、总LRP6和胞质β-连环蛋白的水平,导致Wnt靶标基因Axin2和Survivin的表达降低,表明石斛酚是Wnt/β-catenin通路的新型抑制剂,它能通过下调乳腺癌细胞中磷酸化的LRP6和胞质β-连环蛋白来抑制Wnt/β-连环蛋白信号传导,抑制乳腺癌细胞MDA-MB-231和MDA-MB-468的活力和迁移能力。铁皮石斛提取物可通过激活线粒体凋亡途径和诱导Wnt/β-catenin通路的抑制来抑制肝癌SMMC-7721、BEL-7404细胞和原发性肝癌细胞的增殖(Guo et al.,2019)。新西兰牡荆苷Ⅱ是铁皮石斛抗肿瘤转移的最重要成分之一。新西兰牡荆苷Ⅱ通过使TGF-β/Smad和PI3K/Akt/mTOR通路失活来抑制转化生长因子TGF-β1诱导的肺腺癌A549和H1299细胞的上皮间质转化EMT表型,是阻遏肺腺癌转移的抑制剂(Luo et al.,2019);通过调控MAPK信号通路和Bax/Bcl-2途径诱导肝癌HepG2细胞发生凋亡(罗颖懿等,2019)。铁皮石斛叶提取物异佛来心苷可通过靶向调节TGF-β/Smad和PI3K/Akt/mTOR通路,抑制HepG2和Bel-7402肝癌细胞中TGF-β1诱导的EMT表型,能明显降低肝癌细胞迁移和入侵能力(Xing et al.,2018a)。

4 展望

据全球肿瘤统计分析结果,2018年全球预计有1 810万癌症新发病例和960万癌症死亡病例,2018年我国新增病例数占380.4万例、死亡病例数占229.6万例,我国每天有超过1万人确诊癌症,平均每分钟有7个人得癌症(Bray et al.,2018)。化学治疗(化疗)是目前治疗癌症最主要的手段之一,但化疗具有极大的毒副作用,目前还没有可以完全攻克癌症的有效治疗方法,传统中医药的抗肿瘤作用逐步引起重视。近年来,党和政府高度重视中医药工作,随着系列中医药政策文件的发布,中医药发展已上升为国家战略。石斛是我国名贵的中药材,被誉为“九大仙草”之首,近年来国内外对石斛在抗肿瘤活性成分和抗肿瘤机制方面的研究越来越多。中国石斛属植物中被认定有药用价值的种类已超过50种(曾宋君,2015)。药材来源广泛,活性成分复杂,抗肿瘤研究存在作用机制多、靶点广等特点,只有进一步深入研究,才能为研发石斛新型抗肿瘤药品,为更合理、有效地利用我国宝贵的石斛资源提供科学依据。研究工作可从以下方面开展:(1)目前开展的抗肿瘤活性研究主要集中于铁皮石斛、金钗石斛、鼓槌石斛、叠鞘石斛、束花石斛、霍山石斛等少数石斛属物种,石斛属药用种质资源及其药用价值有待进一步发掘。(2)石斛抗肿瘤活性成分的研究多为总提取物和一级结构分析,构效关系研究較少,需要进一步探索和解析活性成分的作用机理和物质结构之间的关系。(3)石斛属天然产物作为具有生物活性的先导化合物,对其进行结构改造的研究较少,需进一步加强对石斛天然产物的结构改造和活性研究,为后期深入开发石斛类新药做准备。(4)近年来有关石斛属药用次生代谢产物的生物合成途径,特别是其相关调控基因的研究较多但仍不够深入和全面,需进一步利用转录组、基因组、代谢组等多组学技术手段,寻找有效活性成分的关键调控基因和代谢途径,探索提高活性成分表达或异源生物合成途径,促进石斛属资源保护和可持续利用。(5)石斛属植物抗肿瘤药理活性研究多集中在体外细胞和小鼠模型上,体内代谢和吸收机制及体内转化稳定性研究较少,今后在条件成熟的情况下,需开展临床研究。

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