Piezo1 act as a potential oncogene in pancreatic cancer progression.
Piezo1 act as a potential oncogene in pancreatic cancer progression.
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Piezo1 作为胰腺癌进展中的潜在癌基因。
DOI:
10.1016/j.lfs.2022.121035
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发表时间:
2022-10
期刊:
影响因子:
--
通讯作者:
Wang Zheng
中科院分区:
文献类型:
--
作者:
Zhu Zeen;Li Wei;Gong Mengyuan;Wang Lin;Yue Yangyang;Qian Weikun;Zhou Cancan;Duan Wanxing;Han Liang;Li Li;Wu Zheng;Ma Qingyong;Lin Min;Wang Shengpeng;Wang Zheng
Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer related death. A growing number of studies believe that matrix stiffness plays an important role in the development of pancreatic disease. As one of the famous mechanically activated cation channels, Piezo1 has received more attention recently. Here we tried to describe the role of Piezo1 on PDAC progression. It seemed that Piezo1 was a potential tumor-promoting marker of pancreatic cancer. By using Yoda1, we measured the intracellular calcium flux mediated by Piezo1 which confirmed it did act as an intrinsic cation channel in pancreatic cancer cells. Additionally, we also found the inhibition of Piezo1 could inhibit cancer progressionin vitro; however, Piezo1 activation (induced by Yoda1) had an oppositive effect. Moreover, Piezo1 activation may also accelerate pancreatic cancer tumor growth/formationviamodulating pancreatic cancer cell-tumor microenvironment interactionsin vivo. We concluded that Piezo1 acted as an oncogenic gene in pancreatic cancer progression. It might be one of promising targets for pancreatic cancer therapy.
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影响因子:
37.3
作者:
Chen K;Qian W;Jiang Z;Cheng L;Li J;Sun L;Zhou C;Gao L;Lei M;Yan B;Cao J;Duan W;Ma Q
通讯作者:
Ma Q
影响因子:
14.9
作者:
Ritchie ME;Phipson B;Wu D;Hu Y;Law CW;Shi W;Smyth GK
通讯作者:
Smyth GK
影响因子:
25
作者:
Koser DE;Thompson AJ;Foster SK;Dwivedy A;Pillai EK;Sheridan GK;Svoboda H;Viana M;Costa LD;Guck J;Holt CE;Franze K
通讯作者:
Franze K
影响因子:
16.6
作者:
Cox CD;Bae C;Ziegler L;Hartley S;Nikolova-Krstevski V;Rohde PR;Ng CA;Sachs F;Gottlieb PA;Martinac B
通讯作者:
Martinac B
影响因子:
29.4
作者:
Liu M;Zhang Y;Yang J;Cui X;Zhou Z;Zhan H;Ding K;Tian X;Yang Z;Fung KA;Edil BH;Postier RG;Bronze MS;Fernandez-Zapico ME;Stemmler MP;Brabletz T;Li YP;Houchen CW;Li M
通讯作者:
Li M