Literature DB >> 26252941

Diagnostic utility of phosphorylated signal transducer and activator of transcription 5 immunostaining in the diagnosis of mammary analogue secretory carcinoma of the salivary gland: A comparative study of salivary gland cancers.

Akihiko Kawahara1, Tomoki Taira1, Hideyuki Abe1, Yorihiko Takase1, Takashi Kurita2, Eiji Sadashima3,4, Satoshi Hattori3, Ichio Imamura5, Shinji Matsumoto6, Hitomi Fujisaki7, Kazunobu Sueyoshi7, Jun Akiba8, Masayoshi Kage1.   

Abstract

BACKGROUND: Mammary analogue secretory carcinoma (MASC) with an ETS variant gene 6 (ETV6)-neurotrophic tyrosine kinase receptor type 3 (NTRK3) translocation is a newly described type of salivary gland cancer. It is known that overexpression of signal transducer and activator of transcription 5a (STAT5a) occurs in secretory carcinoma of the breast and MASC, and STAT5a expression may be related to the ETV6-NTRK3 translocation. It was hypothesized that phosphorylated signal transducer and activator of transcription 5 (p-STAT5) might be specifically expressed in MASC of the salivary gland.
METHODS: The expression of p-STAT5 and mammaglobin (MMG) was examined with immunohistochemistry (IHC)/immunocytochemistry (ICC) in tissue sections from 58 salivary gland cancers (8 MASCs and 50 other salivary gland cancers) and in cytological smears from 17 salivary gland cancers (7 MASCs with paired histologic samples and 10 other salivary gland cancers).
RESULTS: p-STAT5 IHC was clearly increased in MASC versus normal salivary gland tissue and other salivary gland cancers. p-STAT5 expression was found in 7 of 8 MASCs (87.5%) and in none of the 50 other salivary gland cancers (0%) by IHC. On cytology, p-STAT5 expression was found in all cases of MASC (7 of 7 or 100%) but in none of the 10 other salivary gland cancers (0%) by ICC. The expression rate of MMG by histology and cytology was higher than that of p-STAT5 in the other salivary gland cancers.
CONCLUSIONS: p-STAT5 might be useful as a detection marker of MASC in the differential diagnosis of salivary gland cancers, and initial screening with p-STAT5 IHC/ICC, combined with auxiliary fluorescence in situ hybridization confirmation, is a reliable, economical approach to identifying MASC of the salivary gland.
© 2015 American Cancer Society.

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Keywords:  ETS variant gene 6-neurotrophic tyrosine kinase receptor type 3 (ETV6-NTRK3); immunohistochemistry; mammaglobin; mammary analogue secretory carcinoma; phosphorylated signal transducer and activator of transcription 5 (p-STAT5); salivary gland tumor

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Year:  2015        PMID: 26252941     DOI: 10.1002/cncy.21594

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


  4 in total

1.  Cytomorphologic features of intraductal salivary gland carcinoma: A multi-institutional study of 13 FNA cases with histologic, molecular, and clinical correlations.

Authors:  Kartik Viswanathan; Peter M Sadow; Zahra Maleki; Michiya Nishino; Zubair W Baloch; Todd E Abbott; Rema Rao; William C Faquin
Journal:  Cancer Cytopathol       Date:  2021-10-01       Impact factor: 4.264

2.  Usefulness of immunohistochemistry to distinguish between secretory carcinoma and acinic cell carcinoma in the salivary gland.

Authors:  Yuichiro Hamamoto; Hiroshi Harada; Masaharu Kohara; Keiichiro Honma; Shin-Ichi Nakatsuka; Eiichi Morii
Journal:  Med Mol Morphol       Date:  2020-06-01       Impact factor: 2.070

3.  Etv6 activates vegfa expression through positive and negative transcriptional regulatory networks in Xenopus embryos.

Authors:  Lei Li; Rossella Rispoli; Roger Patient; Aldo Ciau-Uitz; Catherine Porcher
Journal:  Nat Commun       Date:  2019-03-06       Impact factor: 14.919

4.  Clinicopathological investigation of secretory carcinoma cases including a successful treatment outcome using entrectinib for high-grade transformation: a case report.

Authors:  Kensuke Suzuki; Hiroshi Harada; Masayuki Takeda; Chisato Ohe; Yoshiko Uemura; Akihiko Kawahara; Shunsuke Sawada; Akira Kanda; Bhaswati Sengupta; Hiroshi Iwai
Journal:  BMC Med Genomics       Date:  2022-01-06       Impact factor: 3.063

  4 in total

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