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Expression of Transgenes in Native Bladder Urothelium Using Adenovirus-Mediated Transduction
Published on: October 6, 2022
Infection-driven bladder carcinogenesis: Molecular mechanisms of pathogen-urothelial cell interactions
Feifan Tang1, Songbai Liao1, Xianliang Hou2
1Department of Urology, the Nanxishan Hospital of Guangxi Zhuang Autonomous Region, Guilin 541002, China.
Infections from pathogens like Schistosoma haematobium and Human papillomavirus (HPV) are increasingly linked to bladder cancer (BC) development. Further research is needed to understand these complex host-pathogen interactions in BC pathogenesis.
Area of Science:
- Oncology
- Infectious Diseases
- Urology
Background:
- Bladder cancer (BC) is a common genitourinary malignancy.
- The role of infectious agents in BC etiology has been historically underestimated.
- Evidence suggests pathogens like Schistosoma haematobium, HPV, UPEC, and BK virus contribute to BC.
Purpose of the Study:
- To review current knowledge on infection-driven bladder cancer pathogenesis.
- To identify gaps in understanding host-pathogen interactions in BC.
- To consolidate insights into the mechanisms by which infections initiate and progress BC.
Main Methods:
- Literature review of existing studies on infectious agents and bladder cancer.
- Analysis of proposed molecular mechanisms for pathogen-induced carcinogenesis.
- Synthesis of current understanding and identification of research gaps.
Main Results:
- Schistosoma haematobium promotes squamous cell carcinoma via iNOS-mediated DNA damage.
- HPV contributes to oncogenesis through p53 degradation, Rb inactivation, and telomerase activation.
- Recurrent UPEC infections facilitate carcinogenesis via chronic inflammation and genotoxic damage.
Conclusions:
- Infectious agents play a significant, though often underestimated, role in bladder cancer development.
- Detailed mechanistic insights into host-pathogen interactions are crucial for understanding BC pathogenesis.
- Further research is warranted to elucidate these complex relationships and inform prevention/treatment strategies.
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