Literature DB >> 31436913

Insulinoma-associated protein 1 is a novel diagnostic marker of small cell lung cancer in bronchial brushing and cell block cytology from pleural effusions: Validity and reliability with cutoff value.

Hideyuki Abe1, Yorihiko Takase1, Eiji Sadashima2, Chihiro Fukumitsu1, Kazuya Murata1, Takaaki Ito3, Akihiko Kawahara1, Yoshiki Naito1, Jun Akiba1.   

Abstract

BACKGROUND: In recent years, insulinoma-associated protein 1 (INSM1) has been shown to be a key regulator of neuroendocrine development, and it has been evaluated for diagnostic use in some organs.
METHODS: To evaluate the relationship between INSM1 and synaptophysin, and to confirm the cutoff value using receiver operating characteristic curve (ROC) analysis, the authors performed INSM1 immunocytochemistry using cell block (CB) samples from 53 cases of bronchial brushings and 32 cases of pleural effusions (29 small cell lung cancer [SCLC] specimens and 56 non-small cell lung cancer specimens). The marker expression ratio was calculated by counting the positive tumor cells, and the tumor proportion score (TPS) was applied.
RESULTS: INSM1 was expressed in all SCLC specimens, but generally was expressed in <10% of tumor cells in adenocarcinomas. In bronchial brushing samples of SCLC, the INSM1 TPS was 37.5% (staining of >50%), 25.0% (staining of 25%-50%), 29.5% (staining of 10%-25%), and 8.3% (staining of 1%-10%). There were 3 cases (12.5%) with no detectable synaptophysin expression, although the correlation between nuclear INSM1 expression and cytoplasmic synaptophysin expression was statistically significant (P < .001). Receiver operating characteristic curve analysis indicated that 8.68% was the best cutoff value for INSM1, and the sensitivity and specificity between SCLC and non-small cell lung cancer for expression of INSM1 were 95.8% and 100.0%, respectively, in bronchial brushing samples at that cutoff value.
CONCLUSIONS: INSM1 is a novel diagnostic marker for SCLC, and is useful in both bronchial brushing and pleural effusion cytology specimens. Because INSM1 generally is expressed in <10% of tumor cells in adenocarcinomas, determining an accurate cutoff value for INSM1 is important in the diagnosis of SCLC.
© 2019 American Cancer Society.

Entities:  

Keywords:  bronchial and pleural cytology; cell block; insulinoma-associated protein 1 (INSM1); lung cancer; small cell lung carcinoma

Mesh:

Substances:

Year:  2019        PMID: 31436913     DOI: 10.1002/cncy.22177

Source DB:  PubMed          Journal:  Cancer Cytopathol        ISSN: 1934-662X            Impact factor:   5.284


  4 in total

Review 1.  Pulmonary Neuroendocrine Cells and Small Cell Lung Carcinoma: Immunohistochemical Study Focusing on Mechanisms of Neuroendocrine Differentiation.

Authors:  Takaaki Ito; Shinji Kudoh; Kosuke Fujino; Mune Sanada; Yuki Tenjin; Haruki Saito; Yuko Nakaishi-Fukuchi; Hiroki Kameyama; Takaya Ichimura; Naoko Udaka; Noritaka Kudo; Akira Matsuo; Younosuke Sato
Journal:  Acta Histochem Cytochem       Date:  2022-05-24       Impact factor: 1.857

2.  Circular RNA circ_0020123 promotes non-small cell lung cancer progression by sponging miR-590-5p to regulate THBS2.

Authors:  Liang Wang; Lantao Zhao; Yonghong Wang
Journal:  Cancer Cell Int       Date:  2020-08-11       Impact factor: 5.722

3.  Clinical Evaluation of Li Brush Endometrial Samplers for Diagnosing Endometrial Lesions in Women With Intrauterine Devices.

Authors:  Lu Han; Sijia Ma; Lanbo Zhao; Yu Liu; Yiran Wang; Xue Feng; Kailu Zhang; Lei Wang; Li Wang; Panyue Yin; Dongxin Liang; Huilian Hou; Guizhi Shi; Qiling Li
Journal:  Front Med (Lausanne)       Date:  2020-11-30

Review 4.  Morphologic and molecular classification of lung neuroendocrine neoplasms.

Authors:  Jasna Metovic; Giuseppe Pelosi; Marco Barella; Fabrizio Bianchi; Paul Hofman; Veronique Hofman; Myriam Remmelink; Izidor Kern; Lina Carvalho; Linda Pattini; Angelica Sonzogni; Giulia Veronesi; Sergio Harari; Fabien Forest; Mauro Papotti
Journal:  Virchows Arch       Date:  2021-01-21       Impact factor: 4.064

  4 in total

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