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CANCER STEM CELLS |
aSurgery Branch, National Cancer Institute, Bethesda, Maryland, USA;
bDepartment of Pathology,
cMolecular Cytogenetics Core Facility,
dDepartment of Medicine,
eDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York, USA
Key Words. Cancer stem cells • Bone marrow • Solid organ cancer • Bone marrow transplantation
Correspondence: Itzhak Avital, M.D., Surgery Branch, National Cancer Institute, Building 10-Hatfield CRC, Room 3-3940, 10 Center Drive, Bethesda, Maryland 20892-1201, USA. Telephone: 301-496-4164; Fax: 301-402-1738; e-mail: avitali{at}mail.nih.gov
Received May 24, 2007;
accepted for publication July 31, 2007.
Disclosure of potential conflicts of interest is found at the end of this article.
First published online in STEM CELLS EXPRESS August 9, 2007.
Bone marrow-derived stem cells have been shown to participate in solid organ repair after tissue injury. Animal models suggest that epithelial malignancies may arise as aberrant stem cell differentiation during tissue repair. We hypothesized that if bone marrow stem cells participate in human neoplasia, then solid organ cancers developing after allogeneic bone marrow transplantation (ABMT) might include malignant cells of donor origin. We identified four male patients who developed solid organ cancers (lung adenocarcinoma, laryngeal squamous cell carcinoma, glioblastoma, and Kaposi sarcoma) after myeloablation, total body irradiation, and ABMT from female donors. Donor-derived malignant cells comprised 2.5%–6% of the tumor cellularity The presence of donor-derived malignant cells in solid organ cancers suggests that human bone marrow-derived stem cells have a role in solid organ cancer's carcinogenesis. However, the nature of this role is yet to be defined.
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