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- W2000735499 abstract "The role of Abelson murine leukemia virus (A-MuLV) in the accelerated development of murine plasmacytomas (PCs) (Potter et al., 1973: Science, 132, 592-594) was studied in a new experimental system. Spleen cells from pristane-treated or untreated BALB/c mice carrying Robertsonian 6;I5 fusion chromosomes were infected in vitro with helper-free A-MuLV overnight and subsequently transplanted into the peritoneal cavity of pristane-treated or untreated BALB/c mice. Donor-derived PCs developed in 4 out of 76 pristane-treated recipients [latent periods: 38-82 (mean 51) days] that had received spleen cells from pristane-treated donors, and also in 2 out of 41 pristane-treated recipients that had received untreated donor-derived spleen cells (latent periods: 65 and 120 days). Three of the PCs in the former and both PCs in the latter group were tested for integration and expression of the v-abl gene, with positive results. This indicates that the spleen contains PC-precursor cells that can be activated by A-MuLV even before the impact of pristane. All 6 donor-origin PCs carried a translocation involving chromosone 15, band D2/3. Four of these corresponded to a typical 12; 15 translocation, one was a variant 6; 15 translocation and the 6th may represent a previously unidentified translocation between chromosome 15 and the λ gene-carrying chromosome 16. No PCs developed among 29 pristane-untreated recipients that had received pristane-treated donor-derived spleen cells. In addition to PCs, monocytic tumors developed in 37 (26%) of all recipients. Their development was independent of pristane treatment of recipients but was particularly frequent in those who had received spleen cells from pristane-treated donors." @default.
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- W2000735499 date "1989-08-15" @default.
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- W2000735499 title "The accelerating role of abelson murine leukemia virus in murine plasmacytoma development:in vitro infection of spleen cells generates donor-type tumors after transfer to pristane-treated BALB/c mice" @default.
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- W2000735499 doi "https://doi.org/10.1002/ijc.2910440227" @default.
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