Shun-Yu Chi

Dr. Shun-Yu Chi


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 April 2020 in Cancers
Verified
Journal Article
Open access
PDF file
CCChen-Kai Chou
Chen-Kai Chou
SCShun-Yu Chi
Shun-Yu Chi
FCFong-Fu Chou
Fong-Fu Chou
SHShun-Chen Huang
Shun-Chen Huang
JWJia-He Wang
Jia-He Wang
Hong-Yo KangHong-Yo Kang
Hong-Yo Kang
Male gender is a risk factor for mortality in patients with papillary thyroid carcinoma (PTC). This study investigated the impact of androgen receptor (AR) gene expression on the clinical features and progression of PTC. The levels of AR mRNA and protein in frozen, formalin-fixed, paraffin-embedded tissue samples from PTC and adjacent normal thyroid tissue were assessed by quantitative real-time polymerase chain reaction and immunohistochemical staining, respectively, and the relationships between AR expression and clinical features were analyzed. The thyroid cancer cell lines, BCPAP and TPC-1, were used to evaluate the effects of AR on the regulation of cell migration, and key epithelial–mesenchymal transition (EMT) markers. AR mRNA expression was significantly higher in normal thyroid tissue from men than women. The sex difference in AR mRNA expression diminished during PTC tumorigenesis, as AR mRNA expression levels were lower in PTC than normal thyroid tissues from both men and women. AR mRNA expression was significantly decreased in PTC patients with higher risk and in those with extrathyroidal extension. Overexpression of AR in BCPAP cells decreased cell migration and repressed the EMT process by down-regulating mRNA expression of N-cadherin, Snail1, Snail2, Vimentin, and TWIST1 and up-regulating E-cadherin gene expression. These results suggest that suppression of the androgen–AR axis may lead to aggressive tumor behavior in patients with PTC.

Verified
Journal Article
Open access
PDF file
CCChen-Kai Chou
Chen-Kai Chou
SCShun-Yu Chi
Shun-Yu Chi
YHYi-Yung Hung
Yi-Yung Hung
YYYi-Chien Yang
Yi-Chien Yang
HFHung-Chun Fu
Hung-Chun Fu
Hong-Yo KangHong-Yo Kang
Hong-Yo Kang
Papillary thyroid carcinomas (PTC), which is derived from thyroid follicular cells, is the most commonly differentiated thyroid cancer with sex disparity. However, the role of estrogen receptors (ERs) in the pathogenesis of PTC remains unclear. The present study aimed to determine the association of ER mRNA expression levels with clinicopathologic features in PTC. To that aim, the mRNA levels of ESR1 (ERα66), ESR1 (ERα36), ESR2, and G-protein-coupled estrogen receptor 1 (GPER1) in snap-frozen tissue samples from PTCs and adjacent normal thyroid tissues were determined using quantitative reverse transcription polymerase chain reaction (RT-qPCR), and the correlation between ER mRNA expression levels and clinicopathologic features was analyzed. The expression of ERα66, ERα36, ERβ, and GPER1 was lower in PTC specimens than in adjacent normal thyroid tissues. Moreover, low GPER1 expression was associated with extrathyroidal extension. There was no obvious difference in expression of ERs between PTC specimens from male and female patients. In conclusion, our findings highlight the importance of ERs in PTC tumorigenesis.

1 September 2019 in The American Journal of Surgery
Verified
Journal Article
Closed access
FCFong-Fu Chou
Fong-Fu Chou
Jin-Bor ChenJin-Bor Chen
Jin-Bor Chen
SHShun-Cheng Huang
Shun-Cheng Huang
YCYi-Chai Chan
Yi-Chai Chan
SCShun-Yu Chi
Shun-Yu Chi
WCWei-Ting Chen
Wei-Ting Chen

8 May 2020 in World Journal of Surgery
Verified
Journal Article
Closed access
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KWKun-Ta Wu
Kun-Ta Wu
YCYi‐Chia Chan
Yi‐Chia Chan
FCFong‐Fu Chou
Fong‐Fu Chou
YWYi‐Ju Wu
Yi‐Ju Wu
SCShun-Yu Chi
Shun-Yu Chi

1 March 2021 in Journal of Endocrinological Investigation
Verified
Journal Article
Closed access
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Shao-Chun WuShao-Chun Wu
Shao-Chun Wu
SCShun-Yu Chi
Shun-Yu Chi
CRC.-S. Rau
C.-S. Rau
PKP.-J. Kuo
P.-J. Kuo
LHL.-H. Huang
L.-H. Huang
Ching-Hua HsiehChing-Hua Hsieh
Ching-Hua Hsieh

23 February 2023 in Biomedicines
Verified
Journal Article
Open access
PDF file
CLChih-Ying Lee
Chih-Ying Lee
YCYen-Hsiang Chang
Yen-Hsiang Chang
PCPi-Ling Chiang
Pi-Ling Chiang
CWCheng-Kang Wang
Cheng-Kang Wang
ALAn-Ni Lin
An-Ni Lin
WLWei-Che Lin
Wei-Che Lin
Objective: Preoperative localization in patients with primary or secondary hyperparathyroidism before radiofrequency ablation (RFA) is crucial. There is currently a lack of consensus regarding imaging protocol. Evaluating the diagnostic performance of ultrasound, four-dimensional computed tomography (4D-CT), and technetium 99m-sestamibi single-photon-emission-computed tomography/computed tomography (SPECT/CT) is necessary for RFA of hyperparathyroidism. Methods: This retrospective study recruited patients with primary or secondary hyperparathyroidism who underwent ultrasound, 4D-CT, and SPECT/CT before RFA at a single institution. The sensitivity, accuracy, and receiver operating characteristic curve analysis were used to evaluate the diagnostic performance of the imaging modalities. Results: A total of 33 patients underwent RFA for hyperparathyroidism (8 patients with primary hyperparathyroidism, 25 patients with secondary hyperparathyroidism). Ultrasound had the highest sensitivity (0.953) and accuracy (0.943), while 4D-CT had higher sensitivity and accuracy than SPECT/CT (sensitivity/accuracy, 4D-CT vs. SPECT/CT: 0.929/0.920 vs. 0.741/0.716). Combined ultrasound with 4D-CT and the three combined modalities achieved equivalent, and the highest, diagnostic performance (sensitivity 1.000, accuracy 0.989). The lesion length and volume were important predictors of the diagnostic performance of 4D-CT and SPECT/CT (area under curve of length in 4D-CT/volume in 4D-CT/length in SPECT/volume in SPECT: 0.895/0.834/0.767/0.761). Conclusion: Combined ultrasound with 4D-CT provides optimal preoperative localization prior to RFA in patients with primary or secondary hyperparathyroidism. The length and volume of parathyroid lesions are determinative of the diagnostic performance of 4D-CT and SPECT/CT.