Effect of Banxia Xiexintang-containing Serum on Epithelial-mesenchymal Transition of Peritoneal Mesothelial Cells Induced by Gastric Cancer-derived Exosomes
|更新时间:2021-10-14
|
Effect of Banxia Xiexintang-containing Serum on Epithelial-mesenchymal Transition of Peritoneal Mesothelial Cells Induced by Gastric Cancer-derived Exosomes
Chinese Journal of Experimental Traditional Medical FormulaeVol. 27, Issue 21, Pages: 19-26(2021)
DONG Jun-gang,LIU Xi-ping,LI Pei-qing,et al.Effect of Banxia Xiexintang-containing Serum on Epithelial-mesenchymal Transition of Peritoneal Mesothelial Cells Induced by Gastric Cancer-derived Exosomes[J].Chinese Journal of Experimental Traditional Medical Formulae,2021,27(21):19-26.
DONG Jun-gang,LIU Xi-ping,LI Pei-qing,et al.Effect of Banxia Xiexintang-containing Serum on Epithelial-mesenchymal Transition of Peritoneal Mesothelial Cells Induced by Gastric Cancer-derived Exosomes[J].Chinese Journal of Experimental Traditional Medical Formulae,2021,27(21):19-26. DOI: 10.13422/j.cnki.syfjx.20212126.
Effect of Banxia Xiexintang-containing Serum on Epithelial-mesenchymal Transition of Peritoneal Mesothelial Cells Induced by Gastric Cancer-derived Exosomes
To investigate the effect of Banxia Xiexintang on the epithelial-mesenchymal transition (EMT) of human peritoneal mesothelial cell line (HMrSV5) induced by gastric cancer-derived exosomes (Exo).
Method
2
Banxia Xiexintang-containing serum was prepared and the human gastric cancer NCI-N87-derived exosomes (NCI-N87-Exo) were extracted, followed by their identification by transmission electron microscopy and Western blotting and labeling with 1,1-dioctadecyl-3,3,3,3- tetramethylindocarbocyanine perchlorate (Dil). The cells were divided into the blank group, model group, and low-, medium-, and high-dose (13.5,27,54 g·kg
-1
) Banxia Xiexintang groups. HMrSV5 cells in the blank group were cultured alone, the ones in the model group with 100 mg·L
-1
NCI-N87-Exo, and those in the low-, medium-, and high-dose Banxia Xiexintang groups with 100 mg·L
-1
NCI-N87-Exo plus low-, medium-, and high-dose 10% Banxia Xiexintang-containing serum, respectively. Confocal laser microscope was used to observe the uptake of NCI-N87-Exo by HMrSV5 cells at 24 h, 48 h and 72 h. Seventy-two hours later, the morphological changes in HMrSV5 cells were observed. The protein expression levels of E-cadherin, cytokeratin 19 (CK19),
α
-smooth muscle actin (
α
-SMA), elastin, and transforming growth factor-
β
1
(TGF-
β
1
), Smad2/3, and p-Smad2/3 were assayed by Western blot.
Result
2
It was observed under the transmission electron microscope that NCI-N87-Exo showed an oval or dish-shaped vesicle structure with a particle size ranging from 40 to 80 nm. Exo marker proteins CD9 and CD63 were highly expressed while calreticulin was not expressed, implying that the NCI-N87-Exo was confirmed. After 24 h, 48 h, 72 h of co-culture, it was observed under the fluorescence microscope that NCI-N87-Exo were taken up by HMrSV5 cells, which was positively correlated with time. Compared with the blank group, Banxia Xiexintang significantly inhibited the uptake of NCI-N87-Exo by HMrSV5 cells, with better effect noticed in the middle- and high-dose Banxia Xiexintang groups(
P
<
0.05,
P
<
0.01). After intervention with Banxia Xiexintang-containing serum, the HMrSV5 cells were arranged densely, and the intercellular space was significantly reduced, with the most obvious changes present in the high-dose Banxia Xiexintang group. Western blot revealed that the protein expression levels of E-cadherin and CK19 in HMrSV5 cells after being intervened with the medium- and high-dose Banxia Xiexintang-containing serum were increased significantly as compared with those in the blank group, whereas the levels of
α
-SMA and Elastin were decreased significantly (
P
<
0.01). Banxia Xiexintang-containing serum at the low, medium, and high doses remarkably down-regulated TGF-
β
1
and p-Smad2/3 protein expression(
P
<
0.05,
P
<
0.01). However, there was no significant change in Smad2/3.
Conclusion
2
NCI-N87-Exo can be taken up by HMrSV5 cells to induce EMT. Banxia Xiexintang can inhibit the uptake of NCI-N87-Exo by HMrSV5 cells and the resulting EMT induced by NCI-N87-Exo, which is related to the regulation of TGF-
β
1
/Smads signaling pathway.
关键词
Keywords
references
RIIHIMÄKI M , HEMMINKI A , SUNDQUIST K , et al . Metastatic spread in patients with gastric cancer [J]. Oncotarget , 2016 , 7 ( 32 ): 52307 - 52316 .
JIN G , SU Y , DONG Q , et al . Arctigenin alleviates TGF-beta1-induced epithelial-mesenchymal transition and PAI-1 expression via AMPK/NF-kappaB pathway in peritoneal mesothelial cells [J]. Biochem Biophys Res Commun , 2019 , 520 ( 2 ): 413 - 419 .
LI Q , LI B , LI Q , et al . Exosomal miR-21-5p derived from gastric cancer promotes peritoneal metastasis via mesothelial-to-mesenchymal transition [J]. Cell Death Dis , 2018 , 9 ( 9 ): 854 - 871 .
SUN Z , XU H M , ZHAO Z Z , et al . Induction of apoptosis in human peritoneal mesothelial cells by gastric cancer cell supernatant promotes peritoneal carcinomatosis [J]. Tumour Biol , 2014 , 35 ( 8 ): 8301 - 8307 .
YAN Y , FU G , YE Y , et al . Exosomes participate in the carcinogenesis and the malignant behavior of gastric cancer [J]. Scand J Gastroenterol , 2017 , 52 ( 5 ): 499 - 504 .
DENG G , QU J , ZHANG Y , et al . Gastric cancer-derived exosomes promote peritoneal metastasis by destroying the mesothelial barrier [J]. FEBS Lett , 2017 , 591 ( 14 ): 2167 - 2179 .
KENNY H A , KRAUSZ T , YAMADA S D , et al . Use of a novel 3D culture model to elucidate the role of mesothelial cells, fibroblasts and extra-cellular matrices on adhesion and invasion of ovarian cancer cells to the omentum [J]. Int J Cancer , 2010 , 121 ( 7 ): 1463 - 1472 .
SHINBO T , FUSHIDA S , TSUKADA T , et al . Protein-bound polysaccharide K suppresses tumor fibrosis in gastric cancer by inhibiting the TGF-beta signaling pathway [J]. Oncol Rep , 2015 , 33 ( 2 ): 553 - 558 .
WU P , WANG J , MAO X , et al . PDCD4 regulates apoptosis in human peritoneal mesothelial cells and promotes gastric cancer peritoneal metastasis [J]. Histol Histopathol , 2021 , 36 ( 4 ): 447 - 457 .
TSUKADA T , FUSHIDA S , HARADA S , et al . The role of human peritoneal mesothelial cells in the fibrosis and progression of gastric cancer [J]. Int J Oncol , 2012 , 41 ( 2 ): 476 - 482 .
GU J , QIAN H , SHEN L , et al . Gastric cancer exosomes trigger differentiation of umbilical cord derived mesenchymal stem cells to carcinoma-associated fibroblasts through TGF-beta/Smad pathway [J]. PLoS One , 2012 , 7 ( 12 ): e52465 .
YU X , SONG H , XIA T , et al . Growth inhibitory effects of three miR-129 family members on gastric cancer [J]. Gene , 2013 , 532 ( 1 ): 87 - 93 .
COLAK S , TEN D P . Targeting TGF-beta Signaling in Cancer [J]. Trends Cancer , 2017 , 3 ( 1 ): 56 - 71 .
Mechanism on Banxia Xiexintang Inducing Ferroptosis in Gastric Cancer Cells Based on Nrf2/GPX4 Signaling Pathway
Mechanism of Banxia Xiexintang in Prevention and Treatment of Gastric Cancer: A Review
Chinese and Western Medicine Treatment of Gastric Cancer via Ferroptosis: A Review
Pharmacokinetic Differences of Seven Components in Different Phases of Banxia Xiexintang in Rats
Related Author
LI Ling
LI Yaxing
WANG Xue
QIU Xiao
GUO Wei
HUANG Hailiang
LIU Xijian
HAN Tao
Related Institution
College of Traditional Chinese Medicine(TCM),Shandong University of TCM
Experimental Center of Shandong University of TCM
School of Rehabilitation, Shandong University of TCM
Gansu Engineering Laboratory for New Products of Traditional Chinese Medicine (TCM), Gansu Key Laboratory of TCM Excavation and Innovative Transformation,Gansu University of Chinese Medicine
The First Clinical Collage, Hainan Medical University