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201.
A fossil Halobates from the Mediterranean and the origin of sea skaters (Hemiptera, Gerridae) 总被引:1,自引:0,他引:1
N. MLLER ANDERSEN ANTONIO FARMA ALESSANDRO MINELLI GIULIANO PICCOLI 《Zoological Journal of the Linnean Society》1994,112(4):479-489
Five species of sea skaters, genus Halobates Eschscholtz, are the only insects to have successfully colonized the open ocean. In addition, 38 species are found in sheltered coastal waters throughout tropical Indo-Pacific. The taxonomy of the genus is relatively well known, and the phylogeneuc relationships between extant species have recently been analysed (using cladistic methods). In the present paper, we describe the first fossil species of sea skaters, Halobates ruffoi sp. no v. from the Eocene deposit 'Pesciara di Bolca', in the province of Verona, northeastern Italy (geological age about 45 Myr). The significance of this fossil in setting the time scale for the reconstructed phylogeny and anagenesis of adaptive features of sea skaters, and in understanding the evolution and historical zoogeography of these marine insects is discussed. 相似文献
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JOHN P. FRUEHAUF SVETLANA ZONIS MOHAMMAD AL-BASSAM AINURA KYSHTOOBAYEVA CHIRANJIB DASGUPTA TATJANA MILOVANOVIC RICARDO J. PARKER ANTONIO C. BUZAID 《Pigment cell & melanoma research》1997,10(4):236-249
L-buthionine-S,R-sulfoximine (BSO) selectively inhibits glutathione (GSH) synthesis. Malignant melanoma may be uniquely dependent on GSH and its linked enzymes, glutathione S-transferase (GST) and GSH-peroxidase, for metabolism of reactive orthoquinones and peroxides produced during melanin synthesis. We compared the in vitro effects of BSO on melanoma cell lines and fresh melanoma specimens (n = 118) with breast and ovarian cell lines and solid tumors (n = 244). IC50 values (μM) for BSO on melanoma, breast and ovarian tumor specimens were 1.9, 8.6, and 29, respectively. The IC90 for melanoma was 25.5 μM, a level 20-fold lower than steady state levels achieved clinically. The sensitivity of individual specimens of melanoma correlated with their melanin content (r = 0.63). BSO synergistically enhanced BCNU activity against melanoma cell lines and human tumors. We followed GSH levels, GST enzyme activity, GST isoenzyme profiles and mRNA levels after BSO. BSO (50 μM) treatment for 48 hr resulted in a 95% decrease in ZAZ and M14 melanoma cell line GSH levels, and a 60% decrease in GST enzyme activity. GST-μ. protein and mRNA levels were significantly reduced in both cell lines. GST expression was unaffected. These data suggest that BSO action on melanoma may be related to GSH depletion, diminishing the capacity to scavenge toxic metabolites produced during melanin synthesis. We report here for the first time that BSO enhancement of alkylator action may be related in part to down regulation of GST. BSO may be a clinically useful adjunct in the treatment of malignant melanoma. 相似文献