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Chan Choi 6 Articles
Adrenal hemangioblastoma
Joo-Yeon Koo, Kyung-Hwa Lee, Joon Hyuk Choi, Ho Seok Chung, Chan Choi
J Pathol Transl Med. 2022;56(3):161-166.   Published online February 28, 2022
DOI: https://doi.org/10.4132/jptm.2021.12.28
  • 2,872 View
  • 140 Download
AbstractAbstract PDF
Hemangioblastoma (HB) is a rare benign tumor that most commonly occurs in the cerebellum. HB is composed of neoplastic stromal cells and abundant small vessels. However, the exact origin of stromal cells is controversial. Extraneural HBs have been reported in a small series, and peripheral HBs arising in the adrenal gland are extremely rare. Herein, we report a case of sporadic adrenal HB in a 54-year-old woman. The tumor was a well-circumscribed, yellow mass measuring 4.2 cm in diameter. Histologically, the tumor was composed of small blood vessels and vacuolated stromal cells with clear cytoplasm. On immunohistochemical stain, the stromal cells were positive for S-100 protein, neuron-specific enolase, and synaptophysin. The tumor did not reveal mutation of VHL alleles. We herein present a case of HB of the adrenal gland and review of the literature.
Yes-Associated Protein Expression Is Correlated to the Differentiation of Prostate Adenocarcinoma
Myung-Giun Noh, Sung Sun Kim, Eu Chang Hwang, Dong Deuk Kwon, Chan Choi
J Pathol Transl Med. 2017;51(4):365-373.   Published online June 9, 2017
DOI: https://doi.org/10.4132/jptm.2017.05.04
  • 6,640 View
  • 183 Download
  • 8 Web of Science
  • 7 Crossref
AbstractAbstract PDF
Background
Yes-associated protein (YAP) in the Hippo signaling pathway is a growth control pathway that regulates cell proliferation and stem cell functions. Abnormal regulation of YAP was reported in human cancers including liver, lung, breast, skin, colon, and ovarian cancer. However, the function of YAP is not known in prostate adenocarcinoma. The purpose of this study was to investigate the role of YAP in tumorigenesis, differentiation, and prognosis of prostate adenocarcinoma.
Methods
The nuclear and cytoplasmic expression of YAP was examined in 188 cases of prostate adenocarcinoma using immunohistochemistry. YAP expression levels were evaluated in the nucleus and cytoplasm of the prostate adenocarcinoma and the adjacent normal prostate tissue. The presence of immunopositive tumor cells was evaluated and interpreted in comparison with the patients’ clinicopathologic data.
Results
YAP expression levels were not significantly different between normal epithelial cells and prostate adenocarcinoma. However, YAP expression level was significantly higher in carcinomas with a high Gleason grades (8–10) than in carcinomas with a low Gleason grades (6–7) (p < .01). There was no statistical correlation between YAP expression and stage, age, prostate-specific antigen level, and tumor volume. Biochemical recurrence (BCR)–free survival was significantly lower in patients with high YAP expressing cancers (p = .02). However high YAP expression was not an independent prognostic factor for BCR in the Cox proportional hazards model.
Conclusions
The results suggested that YAP is not associated with prostate adenocarcinoma development, but it may be associated with the differentiation of the adenocarcinoma. YAP was not associated with BCR.

Citations

Citations to this article as recorded by  
  • Connecting Hippo Pathway and Cytoophidia in Drosophila Posterior Follicle Cells
    Rui-Yu Weng, Lei Zhang, Ji-Long Liu
    International Journal of Molecular Sciences.2024; 25(3): 1453.     CrossRef
  • NEK1-Mediated Phosphorylation of YAP1 Is Key to Prostate Cancer Progression
    Ishita Ghosh, Md Imtiaz Khalil, Rusella Mirza, Judy King, Damilola Olatunde, Arrigo De Benedetti
    Biomedicines.2023; 11(3): 734.     CrossRef
  • Epigenetic Inheritance From Normal Origin Cells Can Determine the Aggressive Biology of Tumor-Initiating Cells and Tumor Heterogeneity
    Jiliang Feng, Dawei Zhao, Fudong Lv, Zhongyu Yuan
    Cancer Control.2022; 29: 107327482210781.     CrossRef
  • A Yes-Associated Protein (YAP) and Insulin-Like Growth Factor 1 Receptor (IGF-1R) Signaling Loop Is Involved in Sorafenib Resistance in Hepatocellular Carcinoma
    Mai-Huong T. Ngo, Sue-Wei Peng, Yung-Che Kuo, Chun-Yen Lin, Ming-Heng Wu, Chia-Hsien Chuang, Cheng-Xiang Kao, Han-Yin Jeng, Gee-Way Lin, Thai-Yen Ling, Te-Sheng Chang, Yen-Hua Huang
    Cancers.2021; 13(15): 3812.     CrossRef
  • Evidence for discrete modes of YAP1 signaling via mRNA splice isoforms in development and diseases
    Jan Vrbský, Vladimir Vinarský, Ana Rubina Perestrelo, Jorge Oliver De La Cruz, Fabiana Martino, Antonio Pompeiano, Valerio Izzi, Ota Hlinomaz, Vladimir Rotrekl, Marius Sudol, Stefania Pagliari, Giancarlo Forte
    Genomics.2021; 113(3): 1349.     CrossRef
  • Up regulation of the Hippo signalling effector YAP1 is linked to early biochemical recurrence in prostate cancers
    Andreas Marx, Aljoscha Schumann, Doris Höflmayer, Elena Bady, Claudia Hube-Magg, Katharina Möller, Maria Christina Tsourlakis, Stefan Steurer, Franziska Büscheck, Till Eichenauer, Till S. Clauditz, Markus Graefen, Ronald Simon, Guido Sauter, Jakob R. Izbi
    Scientific Reports.2020;[Epub]     CrossRef
  • NEK1 Phosphorylation of YAP Promotes Its Stabilization and Transcriptional Output
    Md Imtiaz Khalil, Ishita Ghosh, Vibha Singh, Jing Chen, Haining Zhu, Arrigo De Benedetti
    Cancers.2020; 12(12): 3666.     CrossRef
Hybrid Granular Cell Tumor/Perineurioma
Sung Sun Kim, Yoo Duk Choi, Jae Hyuk Lee, Chan Choi, Chang Soo Park
Korean J Pathol. 2014;48(6):409-412.   Published online December 31, 2014
DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.6.409
  • 9,271 View
  • 55 Download
  • 2 Crossref

Citations

Citations to this article as recorded by  
  • What’s new in nerve sheath tumors
    Anders Meyer, Steven D. Billings
    Virchows Archiv.2020; 476(1): 65.     CrossRef
  • A Rare Perineurioma/Granular Cell Tumor Hybrid Peripheral Nerve Sheath Tumor
    Koorosh Haghayeghi, Gladys Telang, Sonja Chen, Jack Bevivino, Shamlal Mangray, Yiang Hui, Leslie Robinson-Bostom
    The American Journal of Dermatopathology.2020; 42(10): 762.     CrossRef
Cytokeratin-Positive Gastrointestinal Stromal Tumor of Biphasic Morphology: A Case Report
Sung Sun Kim, Yoo Duk Choi, Jae Hyuk Lee, Chan Choi
Korean J Pathol. 2014;48(5):375-378.   Published online October 27, 2014
DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.5.375
  • 6,488 View
  • 35 Download
  • 2 Crossref
PDF

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  • CYTOKERATINS: NOT AN EPITHELIAL ENTITY ANYMORE?
    Geetpriya Kaur, Devicharan Shetty, Seema Sikka, Aparna Pathak
    INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH.2022; : 15.     CrossRef
  • Gastrointestinal stromal tumors of the stomach in a 10-year-old child
    Saeed Nasher, Fayed Al-Yousofy, Faisal Ahmed
    Journal of Pediatric Surgery Case Reports.2021; 74: 102044.     CrossRef
Diagnostic Utility of a Clonality Test for Lymphoproliferative Diseases in Koreans Using the BIOMED-2 PCR Assay
Young Kim, Yoo Duk Choi, Chan Choi, Jong-Hee Nam
Korean J Pathol. 2013;47(5):458-465.   Published online October 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.5.458
  • 8,779 View
  • 80 Download
  • 13 Crossref
AbstractAbstract PDF
Background

A clonality test for immunoglobulin (IG) and T cell receptor (TCR) is a useful adjunctive method for the diagnosis of lymphoproliferative diseases (LPDs). Recently, the BIOMED-2 multiplex polymerase chain reaction (PCR) assay has been established as a standard method for assessing the clonality of LPDs. We tested clonality in LPDs in Koreans using the BIOMED-2 multiplex PCR and compared the results with those obtained in European, Taiwanese, and Thai participants. We also evaluated the usefulness of the test as an ancillary method for diagnosing LPDs.

Methods

Two hundred and nineteen specimens embedded in paraffin, including 78 B cell lymphomas, 80 T cell lymphomas and 61 cases of reactive lymphadenitis, were used for the clonality test.

Results

Mature B cell malignancies showed 95.7% clonality for IG, 2.9% co-existing clonality, and 4.3% polyclonality. Mature T cell malignancies exhibited 83.8% clonality for TCR, 8.1% co-existing clonality, and 16.2% polyclonality. Reactive lymphadenitis showed 93.4% polyclonality for IG and TCR. The majority of our results were similar to those obtained in Europeans. However, the clonality for IGK of B cell malignancies and TCRG of T cell malignancies was lower in Koreans than Europeans.

Conclusions

The BIOMED-2 multiplex PCR assay was a useful adjunctive method for diagnosing LPDs.

Citations

Citations to this article as recorded by  
  • Experiencia en el uso de protocolos Biomed-2 para el estudio de reordenamientos de TCR e inmunoglobulinas en proliferaciones linfoides en el Instituto Nacional de Cancerología, Colombia
    Nicolás Villamizar-Rivera, Natalia Olaya
    Biomédica.2022; 42(Sp. 1): 64.     CrossRef
  • Enhancing diagnosis of T-cell lymphoma using non-recombined T-cell receptor sequences
    Yi-Lin Chen, Chung-Liang Ho, Chen-Yan Hung, Wan-Li Chen, Chen Chang, Yi-Hsin Hou, Jian-Rong Chen, Pin-Jun Chen, Nan-Haw Chow, Wenya Huang, Ya-Ting Hsu, Tsai-Yun Chen, Tsunglin Liu
    Frontiers in Oncology.2022;[Epub]     CrossRef
  • The utility and limitations of B- and T-cell gene rearrangement studies in evaluating lymphoproliferative disorders
    Hadrian Mendoza, Christopher A. Tormey, Henry M. Rinder, John G. Howe, Alexa J. Siddon
    Pathology.2021; 53(2): 157.     CrossRef
  • Combined detection of lymphocyte clonality and MALT1 translocations in bronchoalveolar lavage fluid for diagnosing pulmonary lymphomas
    Takashi Kido, Hiroshi Ishimoto, Hiroshi Ishii, Kanako Hara, Mutsumi Ozasa, Hiroki Kawabata, Toshinori Kawanami, Yu Suzuki, Hiroki Yoshikawa, Atsuko Hara, Noriho Sakamoto, Nobuhiro Matsumoto, Chiharu Yoshii, Junya Fukuoka, Masaki Fujita, Masamitsu Nakazato
    Scientific Reports.2021;[Epub]     CrossRef
  • Differentiation of lymphocytic‐plasmacytic enteropathy and small cell lymphoma in cats using histology‐guided mass spectrometry
    Sina Marsilio, Shelley J. Newman, James Scot Estep, Paula R. Giaretta, Jonathan A. Lidbury, Emma Warry, Andi Flory, Paul S. Morley, Katy Smoot, Erin H. Seeley, Matthew J. Powell, Jan S. Suchodolski, Jörg M. Steiner
    Journal of Veterinary Internal Medicine.2020; 34(2): 669.     CrossRef
  • T-Cell Receptor Rearrangements Determined Using Fragment Analysis in Patients With T-Acute Lymphoblastic Leukemia
    Hyerim Kim, In-Suk Kim, Chulhun L. Chang, Sun-Young Kong, Young Tak Lim, Seom Gim Kong, Eun Hae Cho, Eun-Yup Lee, Ho-Jin Shin, Hyeon Jin Park, Hyeon-Seok Eom, Hyewon Lee
    Annals of Laboratory Medicine.2019; 39(2): 125.     CrossRef
  • Monitoring immunoglobulin heavy chain and T‑cell receptor gene rearrangement in cfDNA as minimal residual disease detection for patients with acute myeloid leukemia
    Ling Zhong, Jiao Chen, Xiaobing Huang, Yanxing Li, Tao Jiang
    Oncology Letters.2018;[Epub]     CrossRef
  • Molecular pathology diagnosis of diffuse large B cell lymphoma using BIOMED-2 clonal gene rearrangements
    Saeid Ghorbian
    Annals of Diagnostic Pathology.2017; 29: 28.     CrossRef
  • Improved clonality detection in B‐cell lymphoma using a semi‐nested modification of the BIOMED‐2 PCR assay for IGH rearrangement: A paraffin‐embedded tissue study
    Yuma Sakamoto, Ayako Masaki, Satsuki Aoyama, Shusen Han, Kosuke Saida, Kana Fujii, Hisashi Takino, Takayuki Murase, Shinsuke Iida, Hiroshi Inagaki
    Pathology International.2017; 67(9): 453.     CrossRef
  • The prognostic significance of monoclonal immunoglobulin gene rearrangement in conjunction with histologic B‐cell aggregates in the bone marrow of patients with diffuse large B‐cell lymphoma
    Yoon Ah Cho, Woo Ick Yang, Jae‐Woo Song, Yoo Hong Min, Sun Och Yoon
    Cancer Medicine.2016; 5(6): 1066.     CrossRef
  • Nasal-type NK/T-cell lymphomas are more frequently T rather than NK lineage based on T-cell receptor gene, RNA, and protein studies: lineage does not predict clinical behavior
    Mineui Hong, Taehee Lee, So Young Kang, Suk-Jin Kim, Wonseog Kim, Young-Hyeh Ko
    Modern Pathology.2016; 29(5): 430.     CrossRef
  • Long-term Tumor-free Survival With Untreated Primary Diffuse Large B-cell Lymphoma of the Tonsil
    Xiaojing Zhang, Yuanyuan Zheng, Jianlan Xie, Jun Zhu, Yuqin Song, Xiaojing Teng, Wei Liu, Yi Ding, Yuhua Huang, Xiaoge Zhou
    American Journal of Surgical Pathology.2015; 39(11): 1493.     CrossRef
  • Evaluation diagnostic usefulness of immunoglobulin light chains (Igκ, Igλ) and incomplete IGH D-J clonal gene rearrangements in patients with B-cell non-Hodgkin lymphomas using BIOMED-2 protocol
    S. Ghorbian, I. Jahanzad, G. R. Javadi, E. Sakhinia
    Clinical and Translational Oncology.2014; 16(11): 1006.     CrossRef
Intravascular Papillary Endothelial Hyperplasia of the Chest Wall Misdiagnosed as a Malignancy on Fine Needle Aspiration
Yoo-Duk Choi, Young Kim, Sung-Sun Kim, Jo-Heon Kim, Jong-Hee Nam, Chan Choi, Chang-Soo Park
Korean J Pathol. 2013;47(5):499-501.   Published online October 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.5.499
  • 6,156 View
  • 40 Download
  • 3 Crossref
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Citations

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  • Intravascular papillary endothelial hyperplasia in the lungs of a wild Korean raccoon dog
    Warisraporn Tangchang, Su-Young Park, Eun-Hye Jung, Dong-Min Lee, Bit-Na Choi, Hyo-Jung Kwon, Hwa-Young Son
    Journal of Veterinary Diagnostic Investigation.2024; 36(1): 112.     CrossRef
  • Extravascular papillary endothelial hyperplasia mimicking soft tissue sarcoma in 2 cats: a potential diagnostic pitfall
    Francesco Godizzi, Mario Caniatti, Elisabetta Treggiari, Giorgio Romanelli, Ugo Bonfanti, Gabriele Ghisleni, Paola Roccabianca
    Journal of Veterinary Diagnostic Investigation.2022; 34(3): 552.     CrossRef
  • Benign soft tissue lesions that may mimic malignancy
    Jessica A. Forcucci, Evelyn T. Bruner, Michael Timothy Smith
    Seminars in Diagnostic Pathology.2016; 33(1): 50.     CrossRef

J Pathol Transl Med : Journal of Pathology and Translational Medicine