Department of Endocrine and Medical Sciences (DiSEM) & Center of Excellence for Biomedical Research, University of Genova, Viale Benedetto XV, 6, 16132 Genova, Italy.
Pituitary. 2011 Jun;14(2):141-7. doi: 10.1007/s11102-010-0271-2.
Thyrotropin-secreting pituitary adenomas (TSHomas) are a rare cause of hyperthyroidism and account for less than 2% of pituitary adenomas. Medical therapy with somatostatin analogues (SSAs) effectively reduces TSH secretion in approximately 80% of patients and induces shrinkage in about 45% of tumors. According with previous data, resistance to SSA treatment might be due to heterogeneity in somatostatin receptors (SSTRs) expression. We report the case of TSHoma in a 41-year-old man treated with octreotide LAR that caused a dramatic decrease of TSH and thyroid hormones and tumor shrinkage already after 3 months of pre-surgical therapy. In search of potential molecular determinants of octreotide effectiveness, we measured, in primary cultures from this tumor, SSTR and dopamine D2 receptor (D2R) expression, and octreotide and/or cabergoline effects on TSH secretion and cell proliferation. SSTR5 and D2R expression was higher than SSTR2. Octreotide significantly inhibited TSH secretion more effectively than cabergoline (P<0.001), whereas the combined treatment was comparable with cabergoline alone. Similarly, octreotide resulted more effective than cabergoline on cell proliferation, while the combination did not show any additive or synergistic effects. In conclusion, the significant antisecretive and antiproliferative effect of octreotide in this patient might be related to the high expression of SSTR5, in the presence of SSTR2. After reviewing the literature, indeed, in line with previous observations, we hypothesize that SSTR5/SSTR2 ratio in TSHomas may represent a useful marker in predicting the outcome of therapy with SSAs. The role of D2R should be further explored considering that the presence of D2R can influence SSTRs functionality.
促甲状腺激素分泌垂体腺瘤(TSHomas)是甲状腺功能亢进的罕见原因,占垂体腺瘤的不到 2%。生长抑素类似物(SSAs)的药物治疗可有效降低约 80%患者的 TSH 分泌,并使约 45%的肿瘤缩小。根据先前的数据,对 SSA 治疗的抵抗可能是由于生长抑素受体(SSTRs)表达的异质性所致。我们报告了一例 41 岁男性 TSHoma 病例,用奥曲肽 LAR 治疗后,TSH 和甲状腺激素明显下降,且在术前治疗 3 个月后肿瘤缩小。为了寻找奥曲肽疗效的潜在分子决定因素,我们在该肿瘤的原代培养物中测量了 SSTR 和多巴胺 D2 受体(D2R)的表达,以及奥曲肽和/或卡麦角林对 TSH 分泌和细胞增殖的影响。SSTR5 和 D2R 的表达高于 SSTR2。奥曲肽对 TSH 分泌的抑制作用明显优于卡麦角林(P<0.001),而联合治疗与单独使用卡麦角林相当。同样,奥曲肽对细胞增殖的作用也优于卡麦角林,而联合治疗没有显示出任何相加或协同作用。总之,奥曲肽在该患者中的显著抗分泌和抗增殖作用可能与 SSTR5 在 SSTR2 存在时的高表达有关。在回顾文献后,我们确实根据先前的观察结果假设,TSHomas 中 SSTR5/SSTR2 比值可能是预测 SSAs 治疗效果的有用标志物。应进一步探讨 D2R 的作用,因为 D2R 的存在可以影响 SSTRs 的功能。