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1.
Distinct genetic alterations and luminal molecular subtype in nested variant of urothelial carcinoma
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L. V. Morozova T. T. Minakova G. M. Tizenberg I. G. Kuznetsov B. A. Trofimov 《Pharmaceutical Chemistry Journal》1989,23(6):507-510
Translated from Khimiko-farmatsevticheskii Zhurnal, Vol. 23, No. 6, pp. 711–713, June, 1989. 相似文献
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In patients with peritonitis, the biological effects of oxygen aeroions reflect the interplay between molecular and cellular
effects manifesting themselves in the inhibition of lipid peroxidation, increased antioxidizing potential of blood plasma,
and decreased aggregating activity of platelets.
Translated fromByulleten' Eksperimental'noi Biologii i Meditsiny, Vol. 124, No. 9, pp. 283–285, September, 1997 相似文献
8.
Yulia Vistoropsky Svetlana Trofimov Ia Pantsulaia Gregory Livshits 《Annals of human genetics》2006,70(6):749-758
In our research we examined the contribution of putative genetic sources on interindividual variation and cross-sectional correlations of several adhesion molecules, including intracellular (ICAM-1) and vascular cell adhesion molecules (VCAM-1) and E-selectin, in a population-based sample of ethnically homogeneous families of European origin. The plasma levels of these molecules were measured in 947 apparently healthy individuals from 217 nuclear families. Quantitative statistical-genetic analysis implementing the model fitting technique revealed significant parent/offspring and sibling correlations (p < 0.01) for all three molecules. The putative genetic effects explained 55.2 ± 7.2% (VCAM-1), 63.3 ± 7.5% (ICAM) and 63.8 ± 8.1% (E-selectin) of the variation. Common family environmental factors also significantly influenced the variation of E-selectin (13%) and VCAM-1 (28.6%). The main results of our bivariate analysis showed that the observed phenotypic correlations between ICAM-1 and VCAM-1, and between ICAM-1 and E-selectin, were mostly attributable to shared environmental factors ( rE = 0.896 and 0.737, respectively; p < 0.01). However, the correlation between VCAM-1 and E-selectin was likely caused by common genetic effects (rG = 0.334, p < 0.05) . Our results show that familial clustering of adhesion molecules is likely due to strong genetic effects, supplemented with shared environmental factors. 相似文献
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Activated status of tumour-infiltrating lymphocytes and apoptosis in testicular seminoma. 总被引:6,自引:0,他引:6
Evgeny Yakirevich Oleg Lefel Yanina Sova Avi Stein Oded Cohen Ofer Ben Izhak Murray B Resnick 《The Journal of pathology》2002,196(1):67-75
Testicular seminoma is characterized by a prominent lymphoid infiltrate and an excellent prognosis. Cytotoxic T-lymphocytes (CTLs) infiltrating seminoma tumour nests constitute a major subset of the lymphoid infiltrate. The objective of this study was to determine whether CTLs express markers of cytotoxic potential and activity and whether the number of activated CTLs correlates with the extent of apoptosis in testicular seminomas, as opposed to non-seminomatous testicular germ cell tumours (NSTGCTs). Twenty cases of pure seminoma as well as 20 cases of NSTGCTs including 16 mixed germ cell tumours (MGCTs) were studied. Immunohistochemistry for the cytotoxic markers TIA-1 (cytotoxic potential) and granzyme B (cytotoxic activity) and the T-cell markers CD3 and CD8 was performed on formalin-fixed, paraffin-embedded sections. The apoptotic index (AI) was determined by the TUNEL method. The number of CD3(+), CD8(+), TIA-1(+), and granzyme B(+) cells in tumour cell nests was markedly increased in testicular seminomas, compared with NSTGCTs (p<0.01). Activated granzyme B(+) cells numbered 25.6+/-5.2 per high power field in seminomas and 8.9+/-3.2, 8.1+/-3.9, and 0.4+/-0.2 for embryonal carcinomas, yolk sac tumours, and immature teratomas, respectively. Double immunohistochemical staining for granzyme B and CD8 revealed that 82.6+/-8.5% of granzyme B-expressing cells were CD8(+). The tumour cell AI was significantly increased in embryonal carcinoma, compared with the seminoma, yolk sac tumour, and immature teratoma subgroups (6.7+/-1.3, 2.3+/-0.3, 3.0+/-1.1, and 2.3+/-1.1, respectively, p<0.001). TUNEL/CD3 double immunostaining revealed that a significant proportion of the apoptotic seminomatous tumour cells were in direct contact with one or more CD3(+) lymphocytes (47.2+/-6.2%). The number of activated granzyme B(+) CTLs showed a strong linear correlation with the AI in the seminoma group (r=0.71, p<0.0001) but not in other subgroups. TUNEL/granzyme B double immunolabelling revealed that a proportion of activated granzyme B(+) lymphocytes (20%) were often seen in close contact with apoptotic tumour cells. The presence of increased numbers of activated cytotoxic lymphocytes in testicular seminomas suggests that apoptotic tumour cell death in this neoplasm may be triggered by cytotoxic granule effectors. This phenomenon may be one of the key host immune mechanisms leading to the excellent prognosis in this tumour. 相似文献
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R. U. Ostrovskaya S. S. Trofimov T. A. Gudasheva N. M. Smol'nikova E. P. Nemova S. V. Krapivin N. M. Savchenko M. L. Tsirenina A. N. Ushakov E. I. Mel'nik A. B. Kampov-Polevoi 《Bulletin of experimental biology and medicine》1990,110(6):1664-1667
Laboratories of Psychopharmacology and Drug Toxicology, Institute of Pharmacology, Academy of Medical Sciences of the USSR. Research Center for Molecular Diagnoses, Ministry of Health of the RSFSR, Moscow. (Presented by Academician of the Academy of Medical Sciences of the USSR A. V. Val'dman.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 110, No. 12, pp. 613–616, December, 1990. 相似文献