Characteristics of stem cells from human neuroblastoma cell lines and in tumors Journal Article
| Authors: | Walton, J. D.; Kattan, D. R.; Thomas, S. K.; Spengler, B. A.; Guo, H. F. ; Biedler, J. L.; Cheung, N. K. V.; Ross, R. A. |
| Article Title: | Characteristics of stem cells from human neuroblastoma cell lines and in tumors |
| Abstract: | Cellular heterogeneity is a hallmark of human neuroblastoma tumors and cell lines. Within a single neuroblastoma are cells from distinct neural crest lineages whose relative abundance is significant for prognosis. We postulate that a self-renewing multipotent tumor stem cell, which gives rise to diverse cell lineages, is the malignant progenitor of this cancer. To test this hypothesis, we have established 22 cloned, phenotypically homogeneous populations of the three major cell types from 17 neuroblastoma cell lines. In vitro, malignant neuroblastoma stem cells, termed I-type (intermediate type), have distinct morphologic, biochemical, differentiative, and tumorigenic properties, I-type cells express features of both neuroblastic (N) cells (scant cytoplasm, neuritic processes, neurofilaments, pseudoganglia, and granin and neurotransmitter enzyme expression) and substrate-adherent (S) cells (extensive cytoplasm and vimentin and CD44 expression). Moreover, they show bidirectional differentiation to either N or S cells when induced by specific agents. I-type cells are significantly more malignant than N- or S-type cells, with four- to five-fold greater plating efficiencies in soft agar and six-fold higher tumorigenicity in athymic mice. Differences in malignant potential are unrelated to N-myc amplification/overexpression or the ability to digest and migrate through the extracellular matrix. Immunocytochemical analyses of a small series of tumors reveal that frequency of cells coexpressing N and S cell markers correlates with poor prognosis. Thus, I-type stem cells may be instrumental in the genesis and growth of tumors in the patient. Their unique biology deserves attention and further investigation. |
| Keywords: | immunohistochemistry; protein expression; human cell; cancer growth; nonhuman; mouse; phenotype; animals; mice; cell structure; animal experiment; cell differentiation; cancer cell culture; cell line, tumor; cell lineage; stem cell; cell transformation, neoplastic; extracellular matrix; blotting, western; nude mouse; neuroblastoma; immunocytochemistry; neuroblastoma cell; reverse transcriptase polymerase chain reaction; carcinogenicity; cell movement; cytoplasm; stem cells; cell clone; hermes antigen; proto-oncogene proteins c-myc; multipotent stem cell; oncogene c myb; differentiation; vimentin; enzyme; nervous system neoplasms; neurofilament; neural crest cell; tumorigenicity; neurotransmitter; agar; neurite; human neuroblastoma; humans; prognosis; human; female; priority journal; article; i-type cell |
| Journal Title: | NeoPlasia |
| Volume: | 6 |
| Issue: | 6 |
| ISSN: | 1522-8002 |
| Publisher: | Elsevier Science Inc. |
| Date Published: | 2004-11-01 |
| Start Page: | 838 |
| End Page: | 845 |
| Language: | English |
| DOI: | 10.1593/neo.04310 |
| PROVIDER: | scopus |
| PMCID: | PMC1531688 |
| PUBMED: | 15720811 |
| DOI/URL: | |
| Notes: | Neoplasia -- Cited By (since 1996):84 -- Export Date: 16 June 2014 -- CODEN: NEOPF -- Source: Scopus |
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