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67镓在恶性疾病中的定位机制。

The mechanism of 67Ga localization in malignant disease.

作者信息

Weiner R E

机构信息

Nuclear Medicine Department, University of Connecticut Health Center, Farmington 06030, USA.

出版信息

Nucl Med Biol. 1996 Aug;23(6):745-51. doi: 10.1016/0969-8051(96)00119-9.

Abstract

After almost two decades of research, evidence suggests that transferrin receptors are rate-limiting in 67Ga uptake, 67Ga imaging is an in vivo detector of transferring receptors and an indicator of tumor cell proliferation. Moreover, 67Ga can be incorporated into tumor cells by a transferrin receptor-independent process. This pathway could be important in patients with saturated transferrin. Data that appear to support the concept that transferrin receptor-independent transporters are rate-limiting can be resolved by considering the presence of the gallate ion, [67Ga (OH)4]-.

摘要

经过近二十年的研究,有证据表明转铁蛋白受体在67Ga摄取中起限速作用,67Ga成像为转铁蛋白受体的体内探测器及肿瘤细胞增殖指标。此外,67Ga可通过不依赖转铁蛋白受体的过程掺入肿瘤细胞。此途径在转铁蛋白饱和的患者中可能很重要。考虑到镓酸根离子[67Ga(OH)4]-的存在,似乎支持不依赖转铁蛋白受体的转运体起限速作用这一概念的数据就能得到解释。

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