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Hanseong Kim 2 Articles
Mesothelin Expression in Gastric Adenocarcinoma and Its Relation to Clinical Outcomes
Song-Hee Han, Mee Joo, Hanseong Kim, Sunhee Chang
J Pathol Transl Med. 2017;51(2):122-128.   Published online February 15, 2017
DOI: https://doi.org/10.4132/jptm.2016.11.18
  • 7,085 View
  • 162 Download
  • 17 Web of Science
  • 15 Crossref
AbstractAbstract PDF
Background
Although surgical resection with chemotherapy is considered effective for patients with advanced gastric cancer, it remains the third leading cause of cancer-related death in South Korea. Several studies have reported that mesothelial markers including mesothelin, calretinin, and Wilms tumor protein 1 (WT1) were positive in variable carcinomas, associated with prognosis, and were evaluated as potential markers for targeted therapy. The aim of this study was to assess the immunohistochemical expression of mesothelial markers (mesothelin, calretinin, and WT1) in gastric adenocarcinoma and their relations to clinocopathological features and prognosis. Methods: We evaluated calretinin, WT1, and mesothelin expression by immunohistochemical staining in 117 gastric adenocarcinomas. Results: Mesothelin was positively stained in 30 cases (25.6%). Mesothelin expression was related to increased depth of invasion (p = .002), lymph node metastasis (p = .013), and presence of lymphovascular (p = .015) and perineural invasion (p = .004). Patients with mesothelin expression had significantly worse disease-free survival rate compared with that of nonmesothelin expression group (p = .024). Univariate analysis showed that mesothelin expression is related to short-term survival. None of the 117 gastric adenocarcinomas stained for calretinin or WT1. Conclusions: Mesothelin expression was associated with poor prognosis. Our results suggest that mesothelin-targeted therapy should be considered as an important therapeutic alternative for gastric adenocarcinoma patients with mesothelin expression.

Citations

Citations to this article as recorded by  
  • Targeting Mesothelin in Solid Tumours: Anti-mesothelin Antibody and Drug Conjugates
    Quincy Chu
    Current Oncology Reports.2023; 25(4): 309.     CrossRef
  • High expression of mesothelin in plasma and tissue is associated with poor prognosis and promotes invasion and metastasis in gastric cancer
    Suryendu Saha, Chitranjan Mukherjee, Dipjit Basak, Prasun Panja, Pronoy Kanti Mondal, Ranajoy Ghosh, Aniket Halder, Abhijit Chowdhury, Gopal Krishna Dhali, Bitan Kumar Chattopadhyay, Saurabh Ghosh, Somsubhra Nath, Shalini Datta
    Advances in Cancer Biology - Metastasis.2023; 7: 100098.     CrossRef
  • Novel Anti-Mesothelin Nanobodies and Recombinant Immunotoxins with Pseudomonas Exotoxin Catalytic Domain for Cancer Therapeutics
    Minh Quan Nguyen, Do Hyung Kim, Hye Ji Shim, Huynh Kim Khanh Ta, Thi Luong Vu, Thi Kieu Oanh Nguyen, Jung Chae Lim, Han Choe
    Molecules and Cells.2023; 46(12): 764.     CrossRef
  • Immunotherapy for lung cancer: Focusing on chimeric antigen receptor (CAR)-T cell therapy
    Tongqing Xue, Xiang Zhao, Kun Zhao, Yan Lu, Juan Yao, Xianguo Ji
    Current Problems in Cancer.2022; 46(1): 100791.     CrossRef
  • Cellular immunotherapy in gastric cancer: adoptive cell therapy and dendritic cell-based vaccination
    Elnaz Faghfuri, Mahdi Abdoli Shadbad, Amir Hossein Faghfouri, Narges Soozangar
    Immunotherapy.2022; 14(6): 475.     CrossRef
  • Mesothelin Expression in Human Tumors: A Tissue Microarray Study on 12,679 Tumors
    Sören Weidemann, Pauline Gagelmann, Natalia Gorbokon, Maximilian Lennartz, Anne Menz, Andreas M. Luebke, Martina Kluth, Claudia Hube-Magg, Niclas C. Blessin, Christoph Fraune, Katharina Möller, Christian Bernreuther, Patrick Lebok, Till S. Clauditz, Frank
    Biomedicines.2021; 9(4): 397.     CrossRef
  • Host Mesothelin Expression Increases Ovarian Cancer Metastasis in the Peritoneal Microenvironment
    Tyvette S. Hilliard, Brooke Kowalski, Kyle Iwamoto, Elizabeth A. Agadi, Yueying Liu, Jing Yang, Marwa Asem, Yuliya Klymenko, Jeff Johnson, Zonggao Shi, Gifty Marfowaa, Madeleine G. Yemc, Phillip Petrasko, M. Sharon Stack
    International Journal of Molecular Sciences.2021; 22(22): 12443.     CrossRef
  • CAR-T Cell Therapy—An Overview of Targets in Gastric Cancer
    Dominika Bębnowska, Ewelina Grywalska, Paulina Niedźwiedzka-Rystwej, Barbara Sosnowska-Pasiarska, Jolanta Smok-Kalwat, Marcin Pasiarski, Stanisław Góźdź, Jacek Roliński, Wojciech Polkowski
    Journal of Clinical Medicine.2020; 9(6): 1894.     CrossRef
  • Mesothelin-Targeted Recombinant Immunotoxins for Solid Tumors
    Brendan L. Hagerty, Guillaume J. Pegna, Jian Xu, Chin-Hsien Tai, Christine Alewine
    Biomolecules.2020; 10(7): 973.     CrossRef
  • Phase I/II clinical trial of a Wilms’ tumor 1-targeted dendritic cell vaccination-based immunotherapy in patients with advanced cancer
    Wen Zhang, Xu Lu, Peilin Cui, Chunmei Piao, Man Xiao, Xuesong Liu, Yue Wang, Xuan Wu, Jingwei Liu, Lin Yang
    Cancer Immunology, Immunotherapy.2019; 68(1): 121.     CrossRef
  • Mesothelin as a target for cervical cancer therapy
    Korinna Jöhrens, Lea Lazzerini, Jana Barinoff, Jalid Sehouli, Guenter Cichon
    Archives of Gynecology and Obstetrics.2019; 299(1): 211.     CrossRef
  • A targeted proteomics approach reveals a serum protein signature as diagnostic biomarker for resectable gastric cancer
    Qiujin Shen, Karol Polom, Coralie Williams, Felipe Marques Souza de Oliveira, Mariana Guergova-Kuras, Frederique Lisacek, Niclas G. Karlsson, Franco Roviello, Masood Kamali-Moghaddam
    EBioMedicine.2019; 44: 322.     CrossRef
  • Mesothelin as a biomarker for targeted therapy
    Jiang Lv, Peng Li
    Biomarker Research.2019;[Epub]     CrossRef
  • Antibody drug conjugates under investigation in phase I and phase II clinical trials for gastrointestinal cancer
    Alexis D. Leal, Anuradha Krishnamurthy, Lia Head, Wells A. Messersmith
    Expert Opinion on Investigational Drugs.2018; 27(11): 901.     CrossRef
  • Mesothelin‑targeted second generation CAR‑T cells inhibit growth of mesothelin‑expressing tumors in�vivo
    Lin Ye, Yuqing Lou, Liming Lu, Xiaohong Fan
    Experimental and Therapeutic Medicine.2018;[Epub]     CrossRef
Cytologic Findings of Thyroid Carcinoma Showing Thymus-like Differentiation: A Case Report
Sunhee Chang, Mee Joo, Hanseong Kim
Korean J Pathol. 2012;46(3):302-305.   Published online June 22, 2012
DOI: https://doi.org/10.4132/KoreanJPathol.2012.46.3.302
  • 8,736 View
  • 58 Download
  • 13 Crossref
AbstractAbstract PDF

Carcinoma showing thymus-like differentiation (CASTLE) is a rare carcinoma of the thyroid or adjacent soft tissue of the neck with a histologic resemblance to thymic epithelial tumors. Although the fine-needle aspiration (FNA) plays a central role in the initial evaluation of thyroid nodules, few reports about the cytologic findings of CASTLE have been found according to a review of literatures. We report cytologic findings of a case of CASTLE. A 34-year-old woman presented with a 2-month history of sore throat. The FNA showed that the smear was composed of three dimensional clusters and sheets. The tumor cells were round to ovoid with high nuclear : cytoplasmic ratios. The nuclei were vesicular with small nucleoli. There were some tumor cells showing keratinization. Some lymphocytes were found on the background and within clusters. The presence of poorly-differentiated tumor cells with a focal keratinization and a lymphocytic background on the FNA is suggestive of CASTLE.

Citations

Citations to this article as recorded by  
  • Intrathyroidal Thymic Carcinoma: A Retrospective Case Series Study
    Jinhui Liang, Mei Huang, Helang Huang, Li Li, Hailin Luo, Weidong Mao, Shan Gao, Haoxiang Xu
    Ear, Nose & Throat Journal.2023; 102(9): 584.     CrossRef
  • Carcinoma showing thymus‐like differentiation of the parotid gland: The brief report of cytomorphology and review of the literature
    Tomoko Uchiyama, Chiyoko Terada, Yuma Tachibana, Hirokazu Nishiura, Maiko Takeda, Tomomi Fujii, Takahiro Kimura, Masahiro Tsutsumi, Chiho Ohbayashi
    Diagnostic Cytopathology.2023;[Epub]     CrossRef
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    Journal of Surgical Case Reports.2022;[Epub]     CrossRef
  • Ultrasonographic Features of Intrathyroidal Thymic Carcinoma: Review and Analysis of 10 Cases
    Wang, MD Yanhai, Yang, MD Hua, Liu, MD Hanqing, Luo, MD Xiaoli, Liu, BS Luying, Zhou, BS Pingting
    ADVANCED ULTRASOUND IN DIAGNOSIS AND THERAPY.2022; 6(2): 58.     CrossRef
  • Thyroid carcinoma with thymus-like differentiation (CASTLE) tumor: а сase report
    A. A. Ilyin, V. V. Polkin, P. A. Isaev, F. E. Sevrukov, N. Yu. Dvinskych, M. I. Ryzhenkova, S. A. Ivanov, A. D. Kaprin
    Head and Neck Tumors (HNT).2021; 11(2): 64.     CrossRef
  • Metastatic Renal Cell Neoplasm Within a Papillary Thyroid Carcinoma as Incidental Finding in an Asymptomatic Patient: a Case Report
    Maria-Rosa Bella-Cueto, Mireia Pascua-Solé, Albert Cano-Palomares, M. Àngels Cabezuelo-Hernandez, Maria-Rosa Escoda-Giralt, Santiago Barcons-Vilaplana, Paula Serret-Miralles, Carmen Caral-Vanaclocha, Xavier Guirao-Garriga, Joan Prats-Lopez, Meritxell Meda
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    Wen‐hao Ren, Kun Dong, Xiao‐zheng Huang, Yan‐li Zhu
    Diagnostic Cytopathology.2019; 47(11): 1197.     CrossRef
  • Management and Prognostic Factors for Thyroid Carcinoma Showing Thymus-Like Elements (CASTLE): A Case Series Study
    Rui Gao, Xi Jia, Ting Ji, Jinteng Feng, Aimin Yang, Guangjian Zhang
    Frontiers in Oncology.2018;[Epub]     CrossRef
  • Multiple squamous cells in thyroid fine needle aspiration: Friends or foes?
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    Diagnostic Cytopathology.2016; 44(8): 676.     CrossRef
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    WEI GE, YONG-ZHONG YAO, GANG CHEN, YI-TAO DING
    Oncology Letters.2016; 11(2): 1321.     CrossRef
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    Acta Cytologica.2016; 60(5): 421.     CrossRef
  • Carcinoma Showing Thymus-Like Elements of the Thyroid Gland: Report of Three Cases Including One Case with Breast Cancer History
    Guanjun Zhang, Xi Liu, Wei Huang, Xiaofeng Li, Marianne Johnstone, Yuan Deng, Yongqiang Ke, Quentin M. Nunes, Hongyan Wang, Yili Wang, Xuebin Zhang
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J Pathol Transl Med : Journal of Pathology and Translational Medicine