• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

胰腺癌转移、细胞可塑性和 EMT 的分子特征:临床前侵袭性和耐药性的联系。

Molecular profile of metastasis, cell plasticity and EMT in pancreatic cancer: a pre-clinical connection to aggressiveness and drug resistance.

机构信息

Department of Oncology, First Affiliated Hospital, Gannan Medical University, 128 Jinling Road, Ganzhou City, Jiangxi Province, 341000, China.

Department of General Surgery and Institute of Precision Diagnosis and Treatment of Digestive System Tumors, Carson International Cancer Center, Shenzhen University General Hospital, Shenzhen University, Shenzhen, 518055, Guangdong, China.

出版信息

Cancer Metastasis Rev. 2024 Mar;43(1):29-53. doi: 10.1007/s10555-023-10125-y. Epub 2023 Jul 15.

DOI:10.1007/s10555-023-10125-y
PMID:37453022
Abstract

The metastasis is a multistep process in which a small proportion of cancer cells are detached from the colony to enter into blood cells for obtaining a new place for metastasis and proliferation. The metastasis and cell plasticity are considered major causes of cancer-related deaths since they improve the malignancy of cancer cells and provide poor prognosis for patients. Furthermore, enhancement in the aggressiveness of cancer cells has been related to the development of drug resistance. Metastasis of pancreatic cancer (PC) cells has been considered one of the major causes of death in patients and their undesirable prognosis. PC is among the most malignant tumors of the gastrointestinal tract and in addition to lifestyle, smoking, and other factors, genomic changes play a key role in its progression. The stimulation of EMT in PC cells occurs as a result of changes in molecular interaction, and in addition to increasing metastasis, EMT participates in the development of chemoresistance. The epithelial, mesenchymal, and acinar cell plasticity can occur and determines the progression of PC. The major molecular pathways including STAT3, PTEN, PI3K/Akt, and Wnt participate in regulating the metastasis of PC cells. The communication in tumor microenvironment can provide by exosomes in determining PC metastasis. The components of tumor microenvironment including macrophages, neutrophils, and cancer-associated fibroblasts can modulate PC progression and the response of cancer cells to chemotherapy.

摘要

转移是一个多步骤的过程,在此过程中,一小部分癌细胞从肿瘤中脱离,进入血液细胞,以获得转移和增殖的新场所。转移和细胞可塑性被认为是癌症相关死亡的主要原因,因为它们提高了癌细胞的恶性程度,并为患者提供了不良的预后。此外,癌细胞侵袭性的增强与耐药性的发展有关。胰腺癌细胞的转移被认为是患者死亡和预后不良的主要原因之一。胰腺癌是胃肠道最恶性的肿瘤之一,除了生活方式、吸烟和其他因素外,基因组变化在其进展中起着关键作用。EMT 在胰腺癌细胞中的刺激是由于分子相互作用的改变而发生的,除了增加转移外,EMT 还参与了化疗耐药性的发展。上皮细胞、间充质细胞和腺泡细胞的可塑性可以发生,并决定了胰腺癌的进展。包括 STAT3、PTEN、PI3K/Akt 和 Wnt 在内的主要分子途径参与调节胰腺癌细胞的转移。肿瘤微环境中的通讯可以通过外泌体来确定胰腺癌细胞的转移。肿瘤微环境的成分包括巨噬细胞、中性粒细胞和癌症相关成纤维细胞,可以调节胰腺癌的进展和癌细胞对化疗的反应。

相似文献

1
Molecular profile of metastasis, cell plasticity and EMT in pancreatic cancer: a pre-clinical connection to aggressiveness and drug resistance.胰腺癌转移、细胞可塑性和 EMT 的分子特征:临床前侵袭性和耐药性的联系。
Cancer Metastasis Rev. 2024 Mar;43(1):29-53. doi: 10.1007/s10555-023-10125-y. Epub 2023 Jul 15.
2
Paracrine HGF promotes EMT and mediates the effects of PSC on chemoresistance by activating c-Met/PI3K/Akt signaling in pancreatic cancer in vitro.旁分泌 HGF 通过激活胰腺癌细胞中的 c-Met/PI3K/Akt 信号通路促进 EMT,并介导 PSC 对化疗耐药性的影响。
Life Sci. 2020 Dec 15;263:118523. doi: 10.1016/j.lfs.2020.118523. Epub 2020 Oct 8.
3
Annexin A1 Expression Is Associated with Epithelial-Mesenchymal Transition (EMT), Cell Proliferation, Prognosis, and Drug Response in Pancreatic Cancer.膜联蛋白 A1 的表达与胰腺癌中的上皮-间充质转化(EMT)、细胞增殖、预后和药物反应有关。
Cells. 2021 Mar 15;10(3):653. doi: 10.3390/cells10030653.
4
Zinc-Dependent Regulation of ZEB1 and YAP1 Coactivation Promotes Epithelial-Mesenchymal Transition Plasticity and Metastasis in Pancreatic Cancer.锌依赖的 ZEB1 和 YAP1 共激活调控促进胰腺癌上皮-间质转化可塑性和转移。
Gastroenterology. 2021 Apr;160(5):1771-1783.e1. doi: 10.1053/j.gastro.2020.12.077. Epub 2021 Jan 6.
5
microRNA-382 suppresses the progression of pancreatic cancer through the PI3K/Akt signaling pathway by inhibition of Anxa3.miRNA-382 通过抑制 Anxa3 抑制 PI3K/Akt 信号通路抑制胰腺癌的进展。
Am J Physiol Gastrointest Liver Physiol. 2020 Sep 1;319(3):G309-G322. doi: 10.1152/ajpgi.00322.2019. Epub 2020 May 28.
6
MiR-652 inhibits acidic microenvironment-induced epithelial-mesenchymal transition of pancreatic cancer cells by targeting ZEB1.微小RNA-652通过靶向锌指E盒结合蛋白1抑制酸性微环境诱导的胰腺癌细胞上皮-间质转化。
Oncotarget. 2015 Nov 24;6(37):39661-75. doi: 10.18632/oncotarget.5350.
7
Epithelial-to-mesenchymal transition is dispensable for metastasis but induces chemoresistance in pancreatic cancer.上皮-间质转化对胰腺癌转移并非必需,但可诱导其产生化疗耐药性。
Nature. 2015 Nov 26;527(7579):525-530. doi: 10.1038/nature16064. Epub 2015 Nov 11.
8
Molecular mechanisms of pancreatic cancer liver metastasis: the role of PAK2.胰腺癌肝转移的分子机制:PAK2 的作用。
Front Immunol. 2024 Jan 26;15:1347683. doi: 10.3389/fimmu.2024.1347683. eCollection 2024.
9
SPOCK1 promotes metastasis in pancreatic cancer via NF-κB-dependent epithelial-mesenchymal transition by interacting with IκB-α.SPOCK1 通过与 IκB-α 相互作用,通过 NF-κB 依赖性上皮间质转化促进胰腺癌转移。
Cell Oncol (Dordr). 2022 Feb;45(1):69-84. doi: 10.1007/s13402-021-00652-7. Epub 2021 Dec 2.
10
MiR-301a transcriptionally activated by HIF-2α promotes hypoxia-induced epithelial-mesenchymal transition by targeting TP63 in pancreatic cancer.缺氧诱导因子 2α转录激活 miR-301a 通过靶向 TP63 促进胰腺癌缺氧诱导的上皮-间充质转化。
World J Gastroenterol. 2020 May 21;26(19):2349-2373. doi: 10.3748/wjg.v26.i19.2349.

引用本文的文献

1
Unveiling Theranostics: Nanocomplex-Assisted Photodynamic Eradication of Aggressive Cancer Cells and Modulation of Tumor-Associated Macrophages.揭示诊疗一体化:纳米复合物辅助光动力根除侵袭性癌细胞及调节肿瘤相关巨噬细胞
Int J Nanomedicine. 2025 Aug 8;20:9787-9806. doi: 10.2147/IJN.S518050. eCollection 2025.
2
CTHRC1 Derived From Cancer-Associated Fibroblasts Promotes Pancreatic Cancer Progression and Metastasis via the LIF-STAT3 Pathway.源自癌症相关成纤维细胞的CTHRC1通过LIF-STAT3途径促进胰腺癌进展和转移。
Cancer Med. 2025 Aug;14(15):e71126. doi: 10.1002/cam4.71126.
3
Calliviminone A from Induces PANC-1 Pancreatic Cancer Cell Death by Targeting the PI3K/Akt/mTOR Pathway.

本文引用的文献

1
Solasodine suppresses the metastasis of gastric cancer through claudin-2 via the AMPK/STAT3/NF-κB pathway.皂角苷通过 AMPK/STAT3/NF-κB 通路抑制 Claudin-2 抑制胃癌转移。
Chem Biol Interact. 2023 Jul 1;379:110520. doi: 10.1016/j.cbi.2023.110520. Epub 2023 Apr 28.
2
Exosomes in ascites from patients with human pancreatic cancer enhance remote metastasis partially through endothelial-mesenchymal transition.人胰腺癌细胞腹水来源的外泌体部分通过血管内皮-间质转化增强远处转移。
Pancreatology. 2023 Jun;23(4):377-388. doi: 10.1016/j.pan.2023.04.002. Epub 2023 Apr 13.
3
Downregulation of circ-STK39 suppresses pancreatic cancer progression by sponging mir-140-3p and regulating TRAM2-mediated epithelial-mesenchymal transition.
来源于[具体来源未提及]的Calliviminone A通过靶向PI3K/Akt/mTOR信号通路诱导PANC-1胰腺癌细胞死亡。
Plants (Basel). 2025 Jul 7;14(13):2074. doi: 10.3390/plants14132074.
4
Integrated machine learning and single-cell analysis reveal the prognostic and therapeutic potential of SUMOylation-related genes in ovarian cancer.整合机器学习与单细胞分析揭示了SUMO化相关基因在卵巢癌中的预后及治疗潜力。
Front Immunol. 2025 Jun 4;16:1577781. doi: 10.3389/fimmu.2025.1577781. eCollection 2025.
5
Baicalein, a natural flavonoid in gastrointestinal cancers treatment: recent trends and future perspectives.黄芩素,一种用于胃肠道癌症治疗的天然黄酮类化合物:最新趋势与未来展望。
Med Oncol. 2024 Dec 24;42(1):35. doi: 10.1007/s12032-024-02587-z.
6
Cancer-associated fibroblast-derived MMP11 promotes tumor progression in pancreatic cancer.癌症相关成纤维细胞衍生的基质金属蛋白酶11促进胰腺癌的肿瘤进展。
Cancer Sci. 2025 Mar;116(3):643-655. doi: 10.1111/cas.16418. Epub 2024 Dec 5.
7
Apolipoprotein B/Apolipoprotein A1 ratio is an independent prognostic factor in pancreatic cancer.载脂蛋白B/载脂蛋白A1比值是胰腺癌的一个独立预后因素。
Transl Oncol. 2025 Jan;51:102208. doi: 10.1016/j.tranon.2024.102208. Epub 2024 Nov 26.
8
LINC01857 promotes cell proliferation and migration while dampening cell apoptosis in pancreatic cancer by upregulating CDC42EP3 via miR-450b-5p.LINC01857通过miR-450b-5p上调CDC42EP3,从而促进胰腺癌的细胞增殖和迁移,同时抑制细胞凋亡。
Heliyon. 2024 Sep 25;10(21):e38427. doi: 10.1016/j.heliyon.2024.e38427. eCollection 2024 Nov 15.
9
Cetylpyridinium chloride inhibits hepatocellular carcinoma growth and metastasis through regulating epithelial-mesenchymal transition and apoptosis.氯化十六烷基吡啶通过调节上皮-间充质转化和细胞凋亡抑制肝癌生长和转移。
PLoS One. 2024 Sep 20;19(9):e0310391. doi: 10.1371/journal.pone.0310391. eCollection 2024.
10
Recent Treatment Strategies and Molecular Pathways in Resistance Mechanisms of Antiangiogenic Therapies in Glioblastoma.胶质母细胞瘤抗血管生成疗法耐药机制中的最新治疗策略和分子途径
Cancers (Basel). 2024 Aug 27;16(17):2975. doi: 10.3390/cancers16172975.
环状STK39的下调通过海绵化mir-140-3p和调节TRAM2介导的上皮-间质转化来抑制胰腺癌进展。
Apoptosis. 2023 Aug;28(7-8):1024-1034. doi: 10.1007/s10495-023-01813-9. Epub 2023 Apr 11.
4
Ornithine aminotransferase supports polyamine synthesis in pancreatic cancer.鸟氨酸转氨酶支持胰腺癌中的多胺合成。
Nature. 2023 Apr;616(7956):339-347. doi: 10.1038/s41586-023-05891-2. Epub 2023 Mar 29.
5
Circular RNA Fibroblast Growth Factor Receptor 1 Promotes Pancreatic Cancer Progression by Targeting MicroRNA-532-3p/PIK3CB Axis.环状RNA成纤维细胞生长因子受体1通过靶向微小RNA-532-3p/磷脂酰肌醇-3-激酶催化亚基β轴促进胰腺癌进展。
Pancreas. 2022 Sep 1;51(8):930-942. doi: 10.1097/MPA.0000000000002119. Epub 2022 Nov 4.
6
Enhanced Glutaminolysis Drives Hypoxia-Induced Chemoresistance in Pancreatic Cancer.增强的谷氨酰胺分解促进胰腺癌缺氧诱导的化疗耐药性。
Cancer Res. 2023 Mar 2;83(5):735-752. doi: 10.1158/0008-5472.CAN-22-2045.
7
JNK inhibitor IX restrains pancreatic cancer through p53 and p21.JNK抑制剂IX通过p53和p21抑制胰腺癌。
Front Oncol. 2022 Dec 7;12:1006131. doi: 10.3389/fonc.2022.1006131. eCollection 2022.
8
Pancreatic stellate cells exploit Wnt/β-catenin/TCF7-mediated glutamine metabolism to promote pancreatic cancer cells growth.胰腺星状细胞利用 Wnt/β-连环蛋白/TCF7 介导的谷氨酰胺代谢促进胰腺癌细胞生长。
Cancer Lett. 2023 Feb 28;555:216040. doi: 10.1016/j.canlet.2022.216040. Epub 2022 Dec 22.
9
Circ_0018909 knockdown inhibits the development of pancreatic cancer via the miR-545-3p/FASN axis and reduces macrophage polarization to M2.Circ_0018909敲低通过miR-545-3p/FASN轴抑制胰腺癌的发展,并减少巨噬细胞向M2型极化。
J Biochem Mol Toxicol. 2023 Apr;37(4):e23293. doi: 10.1002/jbt.23293. Epub 2022 Dec 21.
10
Circ_0000284 upregulates RHPN2 to facilitate pancreatic cancer proliferation, metastasis, and angiogenesis through sponging miR-1179.环状RNA_0000284通过吸附miR-1179上调RHPN2,以促进胰腺癌的增殖、转移和血管生成。
J Biochem Mol Toxicol. 2023 Mar;37(3):e23274. doi: 10.1002/jbt.23274. Epub 2022 Dec 19.