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Anti-tumor effects of nanosecond pulsed electric fields in a murine model of pancreatic cancer

Liang Yu, Lu Zhou, Hongwei Liu, Qi Huang, Xue-Ting Zheng, Xiao‐An Li, Yan Zhou

2024Bioelectrochemistry11 citationsDOIOpen Access PDF

Abstract

• Nanosecond Pulsed Electric Fields exhibit anti-tumor properties in pancreatic cancer. • Nanosecond Pulsed Electric Fields were associated with key prognostic related genes. • The ceRNA network helps study the mechanisms of Nanosecond Pulsed Electric Fields. Nanosecond Pulsed Electric Fields (nsPEFs) treatment has demonstrated anti-tumor effects on various cancer cell lines. However, the use of this treatment in pancreatic cancer is limited. This study demonstrated that nsPEFs treatment effectively suppressed the proliferation and metastasis of pancreatic cancer cells, while also inducing DNA damage. Meanwhile, animal experiments have shown that nsPEFs effectively suppressed the growth of pancreatic cancer, even in cases where the tumor volume exceeded 500–600 mm 3 at the initiation of treatment. Notably, a single treatment session was found to significantly inhibit tumor growth, while also showing no adverse effects on the main organs of the mice. RNA sequencing and bioinformatics revealed that seven key genes (CDK1, CENPA, UBE2C, CCNB2, PLK1, CCNA2, and CCNB14) were significantly correlated with the overall survival rate of patients with pancreatic cancer. Through the application of the competing endogenous RNA (ceRNA) hypothesis, two miRNAs (has-let-7b-5p and hsa-miR-193b-3p) and four lncRNAs (MIR4435-2HG, ZNF436-AS1, LINC01089, and MIR4435-2HG) were identified as significantly impacting the overall survival of pancreatic cancer patients. We have effectively developed an mRNA-miRNA-lncRNA network that has the potential to stimulate further investigation into the underlying mechanisms of nsPEFs on pancreatic cancer.

Topics & Concepts

Pancreatic cancerCompeting endogenous RNACancer researchmicroRNACancerMetastasisBiologyRNAOncologyMedicineInternal medicineGeneBiochemistryLong non-coding RNAMicroRNA in disease regulationMicrobial Inactivation MethodsCancer-related molecular mechanisms research
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