Over-representation of specific regions of chromosome 22 in cells from human glioma correlate with resistance to 1,3-bis(2-chloroethyl)-1-nitrosourea |
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Authors: | Nicole C Hank Joan Rankin Shapiro Adrienne C Scheck |
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Affiliation: | (1) Neuro-Oncology Research, Barrow Neurological Institute? of St. Joseph's Hospital and Medical Center, 350 W. Thomas Rd, 85013 Phoenix, AZ, USA;(2) Neurosurgery Research, Barrow Neurological Institute? of St. Joseph's Hospital and Medical Center, 350 W. Thomas Rd, 85013 Phoenix, AZ, USA |
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Abstract: | Background Glioblastoma multiforme is the most malignant form of brain tumor. Despite treatment including surgical resection, adjuvant chemotherapy, and radiation, these tumors typically recur. The recurrent tumor is often resistant to further therapy with the same agent, suggesting that the surviving cells that repopulate the tumor mass have an intrinsic genetic advantage. We previously demonstrated that cells selected for resistance to 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) are near-diploid, with over-representation of part or all of chromosomes 7 and 22. While cells from untreated gliomas often have over-representation of chromosome 7, chromosome 22 is typically under-represented. |
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