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Expression of Type 5 Somatostatin Receptor in TSH-secreting Pituitary Adenomas: A Possible Marker for Predicting Long-term Response to Octreotide Therapy

机译:TSH分泌垂体腺瘤中5型生长抑素受体的表达:用于预测奥雷德雷德治疗的长期反应的可能标记

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References(32) Cited-By(18) In TSH-secreting pituitary adenomas (TSHoma), octreotide (OCT) therapy reduces tumor size and TSH secretion in some cases but not in others. As OCT acts through various types of somatostatin receptors (SSTRs), the different responses of TSHoma to OCT might be explained by the differences of SSTR expression. We therefore studied the expression of subtype-specific SSTR mRNA transcripts in tumor tissues by RT-PCR. Type 2 (SSTR2) mRNA transcripts were detected in all 8 tumors but those of SSTR3 and SSTR5 were demonstrated only in 5 of them. Serum TSH levels were decreased by OCT administration test in all patients but OCT therapy was effective in two patients out of three. SSTR5 mRNA was detected in two tumors from the responder, but not in one tumor that was resistant to OCT. These observations suggest that the temporal decrease of TSH by OCT may be mediated by SSTR2, and that the long term response to OCT therapy may be related with the expression of SSTR5. Therefore, the expression of SSTR5 in TSHoma may be a useful marker for predicting the outcome of the therapy, but further studies with larger numbers of patients are necessary.
机译:参考文献(32)在TSH分泌垂体腺瘤(Tshoma)中引用(18),奥曲霉(OCT)治疗在某些情况下减少肿瘤大小和TSH分泌,但不在其他情况下。由于OCT通过各种类型的生长抑素受体(SSTR),可以通过SSTR表达的差异来解释Tsthoma至10月的不同反应。因此,我们通过RT-PCR研究了肿瘤组织中亚型特异性SSTR mRMA转录物的表达。在所有8颗肿瘤中检测到2型(SSTR2)mRNA转录物,但SSTR3和SSTR5的那些仅在其中5中进行了说明。血清TSH水平在所有患者中,OCT给药试验减少,但OCT治疗在三个患者中有效。 SSTR5在来自响应者的两种肿瘤中检测到SSTR5 mRNA,但不在一个抗抵抗OCT的肿瘤中。这些观察结果表明,OCT的TSH的时间降低可能由SSTR2介导,并且长期对OCT治疗的反应可能与SSTR5的表达有关。因此,Tsthoma中SSTR5的表达可以是用于预测治疗结果的有用标记,但需要更多的研究较多的患者。

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