TY - JOUR
T1 - Apoptosis and cell proliferation capacity in AKR lymphoma malignancy variants
AU - Donin, N.
AU - Kay, S.
AU - Sinai, J.
AU - Katzenelson, D.
AU - Siegal, A.
AU - Michowitz, M.
AU - Schibi, G.
AU - Leibovici, J.
PY - 2000
Y1 - 2000
N2 - Dysregulation in apoptotic cell death has recently emerged as a factor in tumorigenesis, but its effect in tumor progression is not yet established. In the present study we evaluated the levels of proliferative and apoptotic cell fractions in a T-cell lymphoma tumor progression model. We compared these features and the expression of apoptosis-related genes in primary tumors of several AKR lymphoma malignancy variants. According to DNA flow cytometry, a considerable proportion of cells (35-40%) was in the proliferative (S + G2/M) phase in all variants, but a slight augmenration with increasing malignancy was noted. Apoptotic cell content was, unexpectedly, the lowest in the less malignant variant. This might be due to the higher content in macrophages observed in this variant, which possibly partly eliminated apoptotic bodies. We found an increase in bcl-2 level with increasing malignancy that was probably counterbalanced by the simultaneous increase observed in the Fas receptor.
AB - Dysregulation in apoptotic cell death has recently emerged as a factor in tumorigenesis, but its effect in tumor progression is not yet established. In the present study we evaluated the levels of proliferative and apoptotic cell fractions in a T-cell lymphoma tumor progression model. We compared these features and the expression of apoptosis-related genes in primary tumors of several AKR lymphoma malignancy variants. According to DNA flow cytometry, a considerable proportion of cells (35-40%) was in the proliferative (S + G2/M) phase in all variants, but a slight augmenration with increasing malignancy was noted. Apoptotic cell content was, unexpectedly, the lowest in the less malignant variant. This might be due to the higher content in macrophages observed in this variant, which possibly partly eliminated apoptotic bodies. We found an increase in bcl-2 level with increasing malignancy that was probably counterbalanced by the simultaneous increase observed in the Fas receptor.
UR - http://www.scopus.com/inward/record.url?scp=0033678861&partnerID=8YFLogxK
U2 - 10.3109/07357900009012202
DO - 10.3109/07357900009012202
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AN - SCOPUS:0033678861
SN - 0735-7907
VL - 18
SP - 702
EP - 714
JO - Cancer Investigation
JF - Cancer Investigation
IS - 8
ER -