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Targeting the Thyroid-Stimulating Hormone Receptor (TSHR) in Thyroid Cancer /

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Targeting the Thyroid-Stimulating Hormone Receptor (TSHR) in Thyroid Cancer // Grayson Robert Gimblet.
作者:	Gimblet, Grayson Robert,
面頁冊數:	1 electronic resource (172 pages)
附註:	Source: Dissertations Abstracts International, Volume: 86-12, Section: B.
提要註:	Radioactive iodine (RAI) has been effective in the treatment of thyroid cancer, the most common endocrine neoplasia, since its introduction into clinical use over eighty years ago. However, not all patients benefit from RAI. Up to 20% of patients with well-differentiated thyroid cancer (WDTC) become radioactive iodine refractory (RAI-R). These RAI-R patients have 5-year survival rates of 50% and 10-year survival rates of 10%. In addition, more aggressive subtypes including oncocytic thyroid carcinoma (OC), poorly differentiated thyroid carcinoma (PDTC), and anaplastic thyroid carcinoma (ATC) are less responsive to RAI therapy. Despite accounting for less than 5% of annual thyroid cancer cases, PDTC and ATC represent more than half of annual thyroid cancer mortality.To address the need for new diagnostic and therapeutic strategies in these patients, this study explores the thyroid-stimulating hormone receptor (TSHR) as an alternative target in thyroid cancer. We described the frequency of TSHR expression in OC (62%), PDTC (58%), and ATC (0%) relative to established expression patterns in WDTC (90%), with particular emphasis placed on expression patterns in RAI-R disease. As thyroid cancer loses endogenous TSHR expression in monolayer cell culture, we established cell lines with stable TSHR expression. We used these cell lines to evaluate TSHR-targeted radiopharmaceuticals. We designed PET radiopharmaceuticals based on two recombinant human thyroid-stimulating hormone analogues, TR1402 and thyrotropin-alfa, radiolabeled with 89Zr (t1/2 = 78.4 h, β+=23%). We performed in vitro assessments of these TSHR-targeted tracers including cell uptake, receptor blocking, internalization, and binding affinity. We evaluated tumor uptake and biodistribution with in vivo PET imaging and ex vivo biodistribution using a subcutaneous xenograft model established in male and female athymic nude mice. The results of these studies show targeting the TSHR is a promising approach for RAI-R and aggressive thyroid cancers. The PET tracers in this study can be used as the basis for future work to design a theranostic TSHR-targeted approach.
Contained By:	Dissertations Abstracts International86-12B.
標題:	Oncology. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=31932654
ISBN:	9798315793366

Targeting the Thyroid-Stimulating Hormone Receptor (TSHR) in Thyroid Cancer /
Gimblet, Grayson Robert,

Targeting the Thyroid-Stimulating Hormone Receptor (TSHR) in Thyroid Cancer /Grayson Robert Gimblet. - 1 electronic resource (172 pages)

Source: Dissertations Abstracts International, Volume: 86-12, Section: B.

Radioactive iodine (RAI) has been effective in the treatment of thyroid cancer, the most common endocrine neoplasia, since its introduction into clinical use over eighty years ago. However, not all patients benefit from RAI. Up to 20% of patients with well-differentiated thyroid cancer (WDTC) become radioactive iodine refractory (RAI-R). These RAI-R patients have 5-year survival rates of 50% and 10-year survival rates of 10%. In addition, more aggressive subtypes including oncocytic thyroid carcinoma (OC), poorly differentiated thyroid carcinoma (PDTC), and anaplastic thyroid carcinoma (ATC) are less responsive to RAI therapy. Despite accounting for less than 5% of annual thyroid cancer cases, PDTC and ATC represent more than half of annual thyroid cancer mortality.To address the need for new diagnostic and therapeutic strategies in these patients, this study explores the thyroid-stimulating hormone receptor (TSHR) as an alternative target in thyroid cancer. We described the frequency of TSHR expression in OC (62%), PDTC (58%), and ATC (0%) relative to established expression patterns in WDTC (90%), with particular emphasis placed on expression patterns in RAI-R disease. As thyroid cancer loses endogenous TSHR expression in monolayer cell culture, we established cell lines with stable TSHR expression. We used these cell lines to evaluate TSHR-targeted radiopharmaceuticals. We designed PET radiopharmaceuticals based on two recombinant human thyroid-stimulating hormone analogues, TR1402 and thyrotropin-alfa, radiolabeled with 89Zr (t1/2 = 78.4 h, β+=23%). We performed in vitro assessments of these TSHR-targeted tracers including cell uptake, receptor blocking, internalization, and binding affinity. We evaluated tumor uptake and biodistribution with in vivo PET imaging and ex vivo biodistribution using a subcutaneous xenograft model established in male and female athymic nude mice. The results of these studies show targeting the TSHR is a promising approach for RAI-R and aggressive thyroid cancers. The PET tracers in this study can be used as the basis for future work to design a theranostic TSHR-targeted approach.

English

ISBN: 9798315793366Subjects--Topical Terms:

273823
Oncology.
Subjects--Index Terms:

Anaplastic thyroid carcinoma

Targeting the Thyroid-Stimulating Hormone Receptor (TSHR) in Thyroid Cancer /
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520 $a Radioactive iodine (RAI) has been effective in the treatment of thyroid cancer, the most common endocrine neoplasia, since its introduction into clinical use over eighty years ago. However, not all patients benefit from RAI. Up to 20% of patients with well-differentiated thyroid cancer (WDTC) become radioactive iodine refractory (RAI-R). These RAI-R patients have 5-year survival rates of 50% and 10-year survival rates of 10%. In addition, more aggressive subtypes including oncocytic thyroid carcinoma (OC), poorly differentiated thyroid carcinoma (PDTC), and anaplastic thyroid carcinoma (ATC) are less responsive to RAI therapy. Despite accounting for less than 5% of annual thyroid cancer cases, PDTC and ATC represent more than half of annual thyroid cancer mortality.To address the need for new diagnostic and therapeutic strategies in these patients, this study explores the thyroid-stimulating hormone receptor (TSHR) as an alternative target in thyroid cancer. We described the frequency of TSHR expression in OC (62%), PDTC (58%), and ATC (0%) relative to established expression patterns in WDTC (90%), with particular emphasis placed on expression patterns in RAI-R disease. As thyroid cancer loses endogenous TSHR expression in monolayer cell culture, we established cell lines with stable TSHR expression. We used these cell lines to evaluate TSHR-targeted radiopharmaceuticals. We designed PET radiopharmaceuticals based on two recombinant human thyroid-stimulating hormone analogues, TR1402 and thyrotropin-alfa, radiolabeled with 89Zr (t1/2 = 78.4 h, β+=23%). We performed in vitro assessments of these TSHR-targeted tracers including cell uptake, receptor blocking, internalization, and binding affinity. We evaluated tumor uptake and biodistribution with in vivo PET imaging and ex vivo biodistribution using a subcutaneous xenograft model established in male and female athymic nude mice. The results of these studies show targeting the TSHR is a promising approach for RAI-R and aggressive thyroid cancers. The PET tracers in this study can be used as the basis for future work to design a theranostic TSHR-targeted approach.
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