mortality/aging
|
• by 56 weeks due to leukemia in pIpC-treated mice
|
hematopoietic system
|
• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
|
|
• in pIpC-treated mice
|
|
• in pIpC-treated mice
|
|
• around the pro-B stage in pIpC-treated mice
|
|
• all pIpC-treated mice develop myeloproliferative disease (MPD)
• Mac-1+/Gr-1+ mature myeloid cells are increased
• 5 of 27 pIpC-treated mice exhibit accelerated MPD
|
|
• hyperproliferation in the liver and spleen in pIpC-treated mice
|
|
• pIpC-treated mice exhibit decreased common myeloid progenitors, granulocyte macrophage progenitors, and megakaryocyte erythroid progenitors compared with wild-type mice
• however, common lymphoid progenitor numbers are normal
|
|
• in pIpC-treated mice
|
|
• extremely high after 32 weeks with leukemia infiltration in nonhematopoietic organs of pIpC-treated mice
|
|
• in pIpC-treated mice
|
|
• 3-fold in the bone marrow in pIpC-treated mice
|
|
• in the spleen of pIpC-treated mice
|
|
• hematopoietic stem cells are hyperactivated in pIpC-treated mice
• hematopoietic stem cell quiescent in pIpC-treated mice is decreased 2-fold while the S and G2/M phase were doubled compared to in wild-type mice
• apoptosis of hematopoietic stem cells in pIpC-treated mice is decreased compared to in wild-type mice
|
neoplasm
|
• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
|
|
• after 12 to 32 weeks of chronic myeloproliferative disease in pIpC-treated mice
|
|
• B and T cell lymphoblastic leukemia/lymphoma in pIpC-treated mice
|
|
• acute myeloid leukemia in 6 of 27 pIpC-treated mice
|
|
• B cell lymphoblastic leukemia/lymphoma in 2 of 27 pIpC-treated mice
|
cellular
aneuploidy
(
J:177285
)
|
• in bone marrow cells and splenocytes from pIpC-treated mice
|
|
• in pIpC-treated mice due to centrosome amplification
|
liver/biliary system
|
• in pIpC-treated mice
|
immune system
|
• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
|
|
• in pIpC-treated mice
|
|
• in pIpC-treated mice
|
|
• around the pro-B stage in pIpC-treated mice
|
|
• all pIpC-treated mice develop myeloproliferative disease (MPD)
• Mac-1+/Gr-1+ mature myeloid cells are increased
• 5 of 27 pIpC-treated mice exhibit accelerated MPD
|
|
• extremely high after 32 weeks with leukemia infiltration in nonhematopoietic organs of pIpC-treated mice
|
|
• in pIpC-treated mice
|
endocrine/exocrine glands
|
• T cell lymphoblastic leukemia/lymphoma in 9 of 27 pIpC-treated mice
|
growth/size/body
|
• in pIpC-treated mice
|
|
• in pIpC-treated mice
|
|
• in pIpC-treated mice
|


Analysis Tools