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基于微小RNA的胰腺癌治疗方法的研发。

Development of microRNA-based therapy for pancreatic cancer.

作者信息

Fesler Andrew, Ju Jingfang

机构信息

Department of Pathology, Stony Brook University, Stony Brook, NY.

出版信息

J Pancreatol. 2019 Dec;2(4):147-151. doi: 10.1097/jp9.0000000000000029.

DOI:10.1097/jp9.0000000000000029
PMID:32133215
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7055707/
Abstract

Despite extensive research efforts on diagnosis and treatment, pancreatic ductal adenocarcinoma (PDAC) remains a devastating disease and the third leading cause of cancer-related death in the United States. Resistance to current therapeutic approaches is a major reason for the poor survival of pancreatic patients. In order to overcome this major challenge and improve patient outcomes, we are in desperate need of novel therapeutic approaches. PDAC chemoresistance mechanisms are complex and multifaceted. Novel therapeutics must be equipped to deal with this challenge. microRNAs (miRNAs) have emerged as strong candidates to fill this role due to their multitargeted function. miRNAs have been shown to have important roles in pancreatic cancer resistance. In this review, we summarize the recent advancement in miRNA research related to PDAC therapeutic resistance mechanisms and the potential of miRNAs as therapeutic agents for future clinical management of PDAC.

摘要

尽管在胰腺癌的诊断和治疗方面进行了广泛的研究,但胰腺导管腺癌(PDAC)仍然是一种极具破坏性的疾病,是美国癌症相关死亡的第三大主要原因。对当前治疗方法的耐药性是胰腺癌患者生存率低的主要原因。为了克服这一重大挑战并改善患者预后,我们迫切需要新的治疗方法。PDAC的化疗耐药机制复杂且多方面。新型疗法必须有能力应对这一挑战。微小RNA(miRNA)因其多靶点功能而成为填补这一角色的有力候选者。已证明miRNA在胰腺癌耐药中发挥重要作用。在本综述中,我们总结了与PDAC治疗耐药机制相关的miRNA研究的最新进展,以及miRNA作为PDAC未来临床管理治疗剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/634e/7055707/46db408a02f3/nihms-1065325-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/634e/7055707/46db408a02f3/nihms-1065325-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/634e/7055707/46db408a02f3/nihms-1065325-f0001.jpg

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本文引用的文献

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2
Exosomal miRNA-106b from cancer-associated fibroblast promotes gemcitabine resistance in pancreatic cancer.肿瘤相关成纤维细胞来源的外泌体 miR-106b 促进胰腺癌对吉西他滨耐药。
Exp Cell Res. 2019 Oct 1;383(1):111543. doi: 10.1016/j.yexcr.2019.111543. Epub 2019 Jul 30.
3
Cancer statistics, 2019.
PTTG1 通过增加 CXADR 表达增强溶瘤腺病毒 5 进入胰腺腺癌细胞。
Viruses. 2023 May 11;15(5):1153. doi: 10.3390/v15051153.
4
MicroRNAs and long non-coding RNAs in pancreatic cancer: From epigenetics to potential clinical applications.胰腺癌中的微小RNA和长链非编码RNA:从表观遗传学到潜在的临床应用
Transl Oncol. 2023 Jan;27:101579. doi: 10.1016/j.tranon.2022.101579. Epub 2022 Nov 1.
5
Long Noncoding RNA and Circular RNA: Two Rising Stars in Regulating Epithelial-Mesenchymal Transition of Pancreatic Cancer.长链非编码RNA与环状RNA:调控胰腺癌上皮-间质转化的两颗新星
Front Oncol. 2022 Jun 3;12:910678. doi: 10.3389/fonc.2022.910678. eCollection 2022.
6
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