Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0030493
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dc.titleChemically-induced cancers do not originate from bone marrow-derived cells
dc.contributor.authorLin H.
dc.contributor.authorHu L.
dc.contributor.authorChen L.
dc.contributor.authorYu H.
dc.contributor.authorWang Q.
dc.contributor.authorChen P.
dc.contributor.authorHu X.-T.
dc.contributor.authorCai X.-J.
dc.contributor.authorGuan X.-Y.
dc.date.accessioned2020-03-18T05:47:03Z
dc.date.available2020-03-18T05:47:03Z
dc.date.issued2012
dc.identifier.citationLin H., Hu L., Chen L., Yu H., Wang Q., Chen P., Hu X.-T., Cai X.-J., Guan X.-Y. (2012). Chemically-induced cancers do not originate from bone marrow-derived cells. PLoS ONE 7 (1) : e30493. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0030493
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/165579
dc.description.abstractBackground: The identification and characterization of cancer stem cells (CSCs) is imperative to understanding the mechanism of cancer pathogenesis. Growing evidence suggests that CSCs play critical roles in the development and progression of cancer. However, controversy exists as to whether CSCs arise from bone marrow-derived cells (BMDCs). Methodology and Principal Findings: In the present study, n-nitrosodiethylamine (DEN) was used to induce tumor formation in female mice that received bone marrow from male mice. Tumor formation was induced in 20/26 mice, including 12 liver tumors, 6 lung tumors, 1 bladder tumor and 1 nasopharyngeal tumor. Through comparison of fluorescence in situ hybridization (FISH) results in corresponding areas from serial tumor sections stained with H&E, we determined that BMDCs were recruited to both tumor tissue and normal surrounding tissue at a very low frequency (0.2-1% in tumors and 0-0.3% in normal tissues). However, approximately 3-70% of cells in the tissues surrounding the tumor were BMDCs, and the percentage of BMDCs was highly associated with the inflammatory status of the tissue. In the present study, no evidence was found to support the existence of fusion cells formed form BMDCs and tissue-specific stem cells. Conclusions: In summary, our data suggest that although BMDCs may contribute to tumor progression, they are unlike to contribute to tumor initiation. © 2012 Lin et al.
dc.publisherPublic Library of Science
dc.sourceUnpaywall 20200320
dc.subjectCD45 antigen
dc.subjectdiethylnitrosamine
dc.subjectvasculotropin receptor 1
dc.subjectcarcinogen
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectarticle
dc.subjectbladder cancer
dc.subjectbone marrow cell
dc.subjectbone marrow derived cell
dc.subjectbone marrow transplantation
dc.subjectcancer tissue
dc.subjectcell expansion
dc.subjectcellular distribution
dc.subjectchemical carcinogenesis
dc.subjectcontrolled study
dc.subjectdisease association
dc.subjectfemale
dc.subjectfluorescence in situ hybridization
dc.subjectinflammation
dc.subjectliver cancer
dc.subjectlung cancer
dc.subjectlymphocyte count
dc.subjectmale
dc.subjectmouse
dc.subjectnasopharynx cancer
dc.subjectnonhuman
dc.subjectprotein expression
dc.subjecttissue section
dc.subjectanimal
dc.subjectbone marrow transplantation
dc.subjectC57BL mouse
dc.subjectcancer stem cell
dc.subjectcell transformation
dc.subjectchemically induced disorder
dc.subjectchromosome aberration
dc.subjectdrug effect
dc.subjectevaluation
dc.subjectmetabolism
dc.subjectneoplasm
dc.subjectpathology
dc.subjectphysiology
dc.subjectsex chromosome
dc.subjectsex chromosome aberration
dc.subjectMus
dc.subjectAbnormal Karyotype
dc.subjectAnimals
dc.subjectBone Marrow Cells
dc.subjectBone Marrow Transplantation
dc.subjectCarcinogens
dc.subjectCell Transformation, Neoplastic
dc.subjectDiethylnitrosamine
dc.subjectFemale
dc.subjectIn Situ Hybridization, Fluorescence
dc.subjectMale
dc.subjectMice
dc.subjectMice, Inbred C57BL
dc.subjectNeoplasms
dc.subjectNeoplastic Stem Cells
dc.subjectSex Chromosome Aberrations
dc.subjectSex Chromosomes
dc.typeArticle
dc.contributor.departmentANATOMY
dc.description.doi10.1371/journal.pone.0030493
dc.description.sourcetitlePLoS ONE
dc.description.volume7
dc.description.issue1
dc.description.pagee30493
dc.published.statePublished
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