Abstract

Simple SummaryBladder cancer is the most common urinary system carcinoma, with more than 430,000 new cases diagnosed every year. More than 25% of patients are classed as having muscle-invasive bladder cancer (MIBC). MIBC is a serious clinical problem and is fatal for the majority of patients. In this work, we focus on the feasibility of plasma-activated saline (PAS) as a potential therapeutic approach for the treatment of MIBC. For this purpose, we evaluated the anticancer effect of PAS on two human bladder cancer cell lines (T24 and J82) in vitro and in vivo. Our initial results demonstrated that the PAS can provide a novel and valuable therapeutic effect for the local treatment of MIBC. We believe that the results presented in this paper will be of interest to many scientists in the field of bladder cancer treatment and plasma biomedicine.Muscle-invasive bladder cancer (MIBC) is a fast-growing and aggressive malignant tumor in urinary system. Since chemotherapy and immunotherapy are only useable with a few MIBC patients, the clinical treatment of MIBC still faces challenges. Here, we examined the feasibility of plasma-activated saline (PAS) as a fledgling therapeutic strategy for MIBC treatment. Our data showed that plasma irradiation could generate a variety of reactive oxygen species (ROS) and reactive nitrogen species (RNS) in saline. In vivo tests revealed that pericarcinomatous tissue injection with PAS was effective at preventing subcutaneous bladder tumor growth, with no side effects to the visceral organs after long-term administration, as well as having no obvious influence on the various biochemistry indices of the blood in mice. The in vitro studies indicated that adding 30% PAS in cell culture media causes oxidative damage to the bladder transitional cells T24 and J82 through enhancing the intracellular ROS level, and eventually induces cancer cells’ apoptosis by activating the ROS-mediated Fas/CD95 pathway. Therefore, for an intracavity tumor, these initial observations suggest that the soaking of the tumor tissue with PAS by intravesical perfusion may be a novel treatment option for bladder cancer.

Highlights

  • Bladder cancer is the most common malignant tumor of the genitourinary system, with a high incidence and recurrence rate in males

  • On account of chemotherapy only being applied for about 50% of muscle-invasive bladder cancer (MIBC) patients due to serious side effects, and the latest immune checkpoint blockade therapy only really working in 15–25% of MIBC patients, the clinical treatment of MIBC still faces challenges

  • Our results revealed that the addition of 30% plasma-activated saline (PAS) in medium can inhibit the viability of both T24 and J82 cells through enhancing the intracellular reactive oxygen species (ROS) level, and trigger cancer cell apoptosis by activating the ROS-mediated Fas/CD95 pathway

Read more

Summary

Introduction

Bladder cancer is the most common malignant tumor of the genitourinary system, with a high incidence and recurrence rate in males. Surgery, radiotherapy, chemotherapy, and biotherapy are the conventional treatments for patients with bladder cancer. Nonmuscle invasive bladder cancer is treated with transurethral bladder tumor resection and subsequent pelvic radiotherapy or intravesical instillation chemotherapy, as well as the bacillus calmette-guerin (BCG) vaccine [4]. Despite the therapeutic strategy usually being conservative, the clinical therapeutic effects for nonmuscle invasive bladder cancer are acceptable. For treatment of muscle-invasive bladder cancer (MIBC), surgical removal and chemotherapy or immunotherapy are preferred because of the inefficiency of radiotherapy [5]. On account of chemotherapy only being applied for about 50% of MIBC patients due to serious side effects, and the latest immune checkpoint blockade therapy only really working in 15–25% of MIBC patients, the clinical treatment of MIBC still faces challenges. New therapies are needed to improve treatments for MIBC

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call