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2000
Volume 5, Issue 4
  • ISSN: 1574-888X
  • E-ISSN: 2212-3946

Abstract

Stem cells are undifferentiated cells that renew themselves while simultaneously producing differentiated tissue- or organspecific cells through asymmetric cell division. The appreciation of the importance of stem cells in normal tissue biology has prompted the idea that cancers may also develop from a progenitor pool (the “cancer stem cell (CSC) hypothesis”), and this idea is gaining increasing acceptance among scientists. CSCs are sub-populations of cancer cells responsible for tumor initiation, differentiation, recurrence, metastasis, and drug resistance. First identified in the hematopoietic system, CSCs have also been discovered in solid tumors of the breast, colon, pancreas, and brain. Recently, the tissue-specific stem cells of the normal urothelium have been proposed to reside in the basal layer, and investigators have isolated phenotypically similar populations of cells from urothelial cancer cell lines and primary tumors. Herein, we review the CSC hypothesis and apply it to explain the development of the two different types of bladder cancer: noninvasive (“superficial”) carcinoma and invasive carcinoma. We also examine potential approaches to identify CSCs in bladder cancer as well as therapeutic applications of these findings. While exciting, the verification of the existence of CSCs in bladder cancer raises several new questions. Herein, we identify and answer some of these questions to help readers better understand bladder cancer development and identify reasonable therapeutic strategy for targeting stem cells.

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/content/journals/cscr/10.2174/157488810793351640
2010-12-01
2025-09-18
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  • Article Type:
    Research Article
Keyword(s): aneuploidy; apical-basal polarity; apoptosis; ATP-binding cassette; basal lamina; binucleate; Bladder cancer; blastocyst; blood circulation; cancer stem cell; cell death; cell-context-dependent manner; cellular detoxification; chromosomal aberrations; chromosomal disorders; chronic myeloid leukemias; clinical realm; colon cancer; colony-forming cells; core circuitry; dehydrogenase isoform; dicer-null; distinct cell types; drug resistance; egg fuse; embryonic stem cells; EMT; epidermal precursors; flow cytometry; genes; genomic sequence; head and neck squamous cell carcinoma; heterogeneity; immunohistochemistry; isolate stem cells; isolation of human bladder; lymphatic vessels; melanomas; mesoderm lineages; migration of cells; miRNA; mononucleated myoblasts; multipotent; multistep process; muscle; muscle invasive; nonembryonic stem cells; noninvasive tumors; nonpolarity; oncogenic/stem cell transcription; organic molecules; ovarian cancer; oxidation of aldehydes; pancreatic cancer; plasticity; polipoid nature; posttranscriptional stage; potency; prostate cancer; protein-encoding; radiotherapeutic measures; renal pelvis; self-renewal transcription factors; side population assay; signaling pathways; spleen; squamous cancer; stem cells; stemness; superficial; superficial tumors; target binding sites; tissues; toxic materials; transcription factors; Transition Between Epithelial and Mesenchymal Phenotype; transitional epithelium; tumor-initiating cell; tumor-stroma interface; tumorigenesis; umbrella cells; urothelium; zygote
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