Lack of expression of ALK and CD30 in breast carcinoma by immunohistochemistry irrespective of tumor characteristics

dc.contributor.authorNassif, Samer R.
dc.contributor.authorEl-Zaatari, Ziad M.
dc.contributor.authorAttieh, Michel
dc.contributor.authorHijazi, Maya M.
dc.contributor.authorFakhreddin, Najla
dc.contributor.authorAridi, Tarek
dc.contributor.authorBoulos, Fouad I.
dc.contributor.authorDing, Jianxun
dc.contributor.departmentPathology and Laboratory Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:10:02Z
dc.date.available2025-01-24T12:10:02Z
dc.date.issued2019
dc.description.abstractCD30 is a member of the tumor necrosis factor family of cell surface receptors normally expressed in lymphocytes, as well as some lymphomas, but has been described in other malignancies. Anaplastic lymphoma kinase (ALK) is a tyrosine kinase receptor that belongs to the insulin receptor superfamily, and is normally expressed in neural cells, but has been detected in several malignancies. There is conflicting data in the literature that describes the expression of these receptors in breast cancer, and the aim of this study is to test the expression of CD30 and ALK in a cohort of Middle Eastern patients with breast carcinoma.Cases of invasive breast cancer from the archives of AUBMC were reviewed over a period of 9 years, and the blocks that were used for immunohistochemical staining for ER, PR, Her-2/neu were selected. Immunohistochemical staining for CD30 (JCM182) and ALK (5A4 and D5F3) was performed.Two hundred eighty-four cases were identified (2 cases were male), with a mean age of 55±12. CD30 and ALK expression was not seen in any of the cases.Our cohort showed complete negativity to both CD30 and ALK, adding to the conflicting data available in the literature, and more studies are needed to reliably identify a trend of expression of CD30 and ALK in breast carcinoma, especially in the Middle East. © 2019 the Author(s). Published by Wolters Kluwer Health, Inc.
dc.identifier.doihttps://doi.org/10.1097/MD.0000000000016702
dc.identifier.eid2-s2.0-85070539546
dc.identifier.pmid31393373
dc.identifier.urihttp://hdl.handle.net/10938/32234
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofMedicine (United States)
dc.sourceScopus
dc.subjectAlk
dc.subjectBreast cancer
dc.subjectCarcinoma
dc.subjectCd30
dc.subjectMiddle east
dc.subjectAdult
dc.subjectAged
dc.subjectAnaplastic lymphoma kinase
dc.subjectBreast neoplasms
dc.subjectCohort studies
dc.subjectFemale
dc.subjectHumans
dc.subjectKi-1 antigen
dc.subjectMale
dc.subjectMiddle aged
dc.subjectEpidermal growth factor receptor 2
dc.subjectEstrogen receptor
dc.subjectImmunoglobulin
dc.subjectProgesterone receptor
dc.subjectTumor necrosis factor receptor superfamily member 8
dc.subjectArticle
dc.subjectBreast carcinoma
dc.subjectHuman
dc.subjectImmunohistochemistry
dc.subjectMajor clinical study
dc.subjectPriority journal
dc.subjectBreast tumor
dc.subjectCohort analysis
dc.subjectMetabolism
dc.subjectPathology
dc.titleLack of expression of ALK and CD30 in breast carcinoma by immunohistochemistry irrespective of tumor characteristics
dc.typeArticle

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