Page 55 - 202015
P. 55
表 7 各组细胞中 IL-6、JAK2、STAT3 蛋白表达水平测 血清对神经胶质瘤 U251 细胞 JAK/STAT 信号通路的影
定结果(x±±s,n=3) 响[J].中国药房,2017,28(16):2176-2179.
Tab 7 Protein expression levels of IL-6,JAK2 and [ 9 ] 谢小倩,李贺,王亚乐,等.龙胆苦苷对佐剂性关节炎大鼠
STAT3 of cells in each group(x±±s,n=3) 的抗炎作用[J].中国实验方剂学杂志,2020,26(6):58-
63.
组别 质量浓度,mg/L IL-6/β-actin JAK2/β-actin STAT3/β-actin
阴性对照组 0.872±0.050 0.805±0.056 0.713±0.028 [10] XIE X,LI H,WANG Y,et al. Therapeutic effects of gen-
吉西他滨组 4 0.302±0.068 ** 0.377±0.028 ** 0.421±0.039 ** tiopicroside on adjuvant-induced arthritis by inhibiting
龙胆苦苷低浓度组 15 0.846±0.051 ## 0.738±0.086 ## 0.681±0.040 ## inflammation and oxidative stress in rats[J]. Int Immu-
龙胆苦苷中浓度组 30 0.547±0.057 **## 0.486±0.050 **# 0.589±0.059 *# nopharmacol,2019. DOI:10.1016/j.intimp.2019.105840.
龙胆苦苷高浓度组 60 0.373±0.058 ** 0.452±0.051 ** 0.449±0.047 **
[11] 王美灵,张雷明,郝妍斐,等.龙胆苦苷对类风湿性关节炎
#
注:与阴性对照组比较, P<0.01;与吉西他滨组比较,P<0.05,
**
的保护作用及其机制[J].中国药理学与毒理学杂志,
## P<0.01
2019,33(9):721.
Note:vs. negative control group, * * P<0.01;vs. gemcitabine
[12] LI X,YANG C,SHEN H. Gentiopicroside exerts convinc-
#
group,P<0.05,P<0.01
##
ing antitumor effects in human ovarian carcinoma cells
胆苦苷可显著抑制 PANC-1 细胞的增殖、生长和克隆形 (SKOV3) by inducing cell cycle arrest,mitochondrial
成 ,促 进 细 胞 凋 亡 ,下 调 细 胞 中 IL-6、JAK2、STAT3 mediated apoptosis and inhibition of cell migration[J]. J
mRNA 及其蛋白表达,并且 60 mg/L 龙胆苦苷的作用与 Buon,2019,24(1):280-284.
4 mg/L吉西他滨的作用相近(吉西他滨是临床上治疗胰 [13] 梁春丽,王峥,李炳,等.姜黄素对人胰腺癌PANC-1细胞
腺癌的基础化疗药物 ,故在本研究中将其设为阳性对 甲基化转移酶表达影响的体外研究[J].上海中医药杂
[21]
照)。 志,2015,49(10):77-79、97.
综上所述,龙胆苦苷对人胰腺癌细胞 PANC-1 具有 [14] KIM JH,CHOI HS,KIM SL,et al. The PAK1-Stat3 sig-
抑制增殖、诱导凋亡的作用,其机制可能与抑制 IL-6/ naling pathway activates IL-6 gene transcription and hu-
JAK2/STAT3 信号通路的激活有关,但其更多的作用机 man breast cancer stem cell formation[J]. Cancers:Basel,
2019,11(10):1527-1546.
制后续需进一步研究。
[15] RAZIDLO GL,BURTON KM,MCNIVEN MA.Interleu-
参考文献
kin-6 promotes pancreatic cancer cell migration by rapid-
[ 1 ] ABBASSI R,SCHMID RM. Evolving treatment paradi-
ly activating the small GTPase CDC42[J]. J Biol Chem,
gms for pancreatic cancer[J]. Visc Med,2019,35(6):
2018,293(28):11143-11153.
362-372. [16] 陈涛,曾永鸿.肿瘤微环境中异常表达的白介素6对肿瘤
[ 2 ] 刘梦奇,吉顺荣,徐晓武,等. 2019 年胰腺癌研究及诊疗
进程的影响[J].解剖学杂志,2016,39(4):501-503.
新进展[J].中国癌症杂志,2020,30(1):1-10.
[17] 任为,牟宜双,许可,等.迷迭香酸通过诱导凋亡及抑制
[ 3 ] WANG Y,YANG G,YOU L,et al. Role of the micro-
NF-κB信号通路发挥抗肝癌作用的机制研究[J].中药药
biome in occurrence,development and treatment of pan-
理与临床,2016,32(2):31-35.
creatic cancer[J]. Mol Cancer,2019,18(1):173-186.
[18] 张曼泽,李峰生,王思念,等. IL-6通过JAK2/STAT3信号
[ 4 ] STONE ML,BEATTY GL. Cellular determinants and thera- 通路促进 CD133-肺腺癌细胞(A549)获得干性特征[J].
peutic implications of inflammation in pancreatic cancer
军事医学,2018,42(9):678-683.
[J]. Pharmacol Ther,2019,201(9):202-213.
[19] LIU Z,CHEN T,LU X,et al. Overexpression of variant
[ 5 ] ZHANG X,LU H,HONG W,et al. Tyrphostin B42 atte-
PNPLA3 gene at I148M position causes malignant trans-
nuates trichostatin A-mediated resistance in pancreatic
formation of hepatocytes via IL-6-JAK2/STAT3 pathway
cancer cells by antagonizing IL-6/JAK2/STAT3 signaling in low dose free fatty acid exposure:a laboratory investi-
[J]. Oncol Rep,2018,39(4):1892-1900.
gation in vitro and in vivo[J]. Am J Transl Res,2016,8
[ 6 ] LIU X,WANG J,WANG H,et al. REG3A accelerates pan-
(3):1319-1338.
creatic cancer cell growth under IL-6-associated inflam-
[20] 李雷雷,郭彬,郭佳培,等.肿瘤相关巨噬细胞通过JAK2/
matory condition:involvement of a REG3A-JAK2/STAT3
STAT3途径调控肝癌细胞凋亡的机制研究[J].现代预防
positive feedback loop[J]. Cancer Lett,2015,362(1):
医学,2017,44(13):2406-2410.
45-60. [21] 彭梦媛,邱峰,黄丹,等.姜黄素对胰腺癌SW1990细胞耐
[ 7 ] ZHAO H,GUO Y,LI S,et al. A novel anti-cancer agent
吉西他滨的逆转作用及机制研究[J].中国药房,2019,30
icaritin suppresses hepatocellular carcinoma initiation and
(9):1192-1197.
malignant growth through the IL-6/JAK2/STAT3 pathway
(收稿日期:2020-02-24 修回日期:2020-06-12)
[J]. Oncotarget,2015,6(31):31927-31943.
(编辑:林 静)
[ 8 ] 刘建民,黄良文,朱旭红,等. 3种活血化瘀中药复方含药
中国药房 2020年第31卷第15期 China Pharmacy 2020 Vol. 31 No. 15 ·1841 ·