» Articles » PMID: 24934485

KRAS, EGFR, PDGFR-α, KIT and COX-2 Status in Carcinoma Showing Thymus-like Elements (CASTLE)

Overview
Journal Diagn Pathol
Publisher Biomed Central
Specialty Pathology
Date 2014 Jun 18
PMID 24934485
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Background: CASTLE (Carcinoma showing thymus-like elements) is a rare malignant neoplasm of the thyroid resembling lymphoepithelioma-like and squamous cell carcinoma of the thymus with different biological behaviour and a better prognosis than anaplastic carcinoma of the thyroid.

Methods: We retrospectively investigated 6 cases of this very rare neoplasm in order to investigate the mutational status of KRAS, EGFR, PDGFR-α and KIT, as well as the immunohistochemical expression pattern of CD117, EGFR and COX-2, and possibly find new therapeutic targets.

Results: Diagnosis was confirmed by a moderate to strong expression of CD5, CD117 and CK5/6, whereas thyroglobulin, calcitonin and TTF-1 were negative in all cases. Tumors were also positive for COX-2 and in nearly all cases for EGFR. In four cases single nucleotide polymorphisms (SNPs) could be detected in exon 12 of the PDGFR-α gene (rs1873778), in three cases SNPs were found in exon 20 of the EGFR gene (rs1050171). No mutations were found in the KIT and KRAS gene.

Conclusions: All tumors showed a COX-2 expression as well as an EGFR expression except for one case and a wild-type KRAS status. No activating mutations in the EGFR, KIT and PDGFR-α gene could be detected. Our data may indicate a potential for targeted therapies, but if these therapeutic strategies are of benefit in CASTLE remains to be determined.

Virtual Slides: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1658499296115016.

Citing Articles

Intra-Operative Tumour Detection and Staging in Pancreatic Cancer Surgery: An Integrative Review of Current Standards and Future Directions.

Kotb A, Hafeji Z, Jesry F, Lintern N, Pathak S, Smith A Cancers (Basel). 2024; 16(22).

PMID: 39594758 PMC: 11592681. DOI: 10.3390/cancers16223803.


TTF-1 is a highly sensitive but not fully specific marker for pulmonary and thyroidal cancer: a tissue microarray study evaluating more than 17,000 tumors from 152 different tumor entities.

Moller K, Gulzar T, Lennartz M, Viehweger F, Kluth M, Hube-Magg C Virchows Arch. 2024; 485(5):815-828.

PMID: 39377914 PMC: 11564378. DOI: 10.1007/s00428-024-03926-1.


Intrathyroid thymic carcinoma: clinicopathological features and whole exome sequencing analysis.

Li J, Xiang R, Li Y, Liao Q, Liu Y Virchows Arch. 2023; 482(5):813-822.

PMID: 37016248 DOI: 10.1007/s00428-023-03536-3.


A Case of Thyroid Carcinoma Showing Thymus-Like Differentiation With Breast Cancer Susceptibility Gene 2 Mutation: A Case Report and Literature Review.

Kuroki M, Shibata H, Iinuma R, Okuda H, Ohashi T, Ogawa T Cureus. 2022; 14(10):e30655.

PMID: 36426335 PMC: 9681707. DOI: 10.7759/cureus.30655.


Genomic variation associated with carcinoma showing thymus-like elements (CASTLE) in thyroid gland.

Jiang L, Zheng W, Chen C Laryngoscope Investig Otolaryngol. 2022; 7(3):894-900.

PMID: 35734076 PMC: 9194970. DOI: 10.1002/lio2.805.


References
1.
Girard N . Thymic tumors: relevant molecular data in the clinic. J Thorac Oncol. 2010; 5(10 Suppl 4):S291-5. DOI: 10.1097/JTO.0b013e3181f209b9. View

2.
Henley J, Cummings O, Loehrer Sr P . Tyrosine kinase receptor expression in thymomas. J Cancer Res Clin Oncol. 2004; 130(4):222-4. DOI: 10.1007/s00432-004-0545-z. View

3.
Alexiev B, Drachenberg C, Burke A . Thymomas: a cytological and immunohistochemical study, with emphasis on lymphoid and neuroendocrine markers. Diagn Pathol. 2007; 2:13. PMC: 1871568. DOI: 10.1186/1746-1596-2-13. View

4.
Miyauchi A, Kuma K, Matsuzuka F, Matsubayashi S, Kobayashi A, Tamai H . Intrathyroidal epithelial thymoma: an entity distinct from squamous cell carcinoma of the thyroid. World J Surg. 1985; 9(1):128-35. DOI: 10.1007/BF01656263. View

5.
Pan C, Chen P, Chiang H . KIT (CD117) is frequently overexpressed in thymic carcinomas but is absent in thymomas. J Pathol. 2004; 202(3):375-81. DOI: 10.1002/path.1514. View