Skip to main content

Advertisement

Log in

Frequent nuclear β-catenin expression in pulmonary enteric-type adenocarcinoma according to the current World Health Organization criteria

  • BRIEF REPORT
  • Published:
Virchows Archiv Aims and scope Submit manuscript

Abstract

Based on the current World Health Organization classification criteria, five of 3895 consecutive cases of surgically resected primary lung carcinomas (0.13%) categorized as enteric-type were analyzed. Three cases completely comprised tumor cells that resemble colorectal adenocarcinoma, while the other two cases exhibited features of conventional adenocarcinomas admixed with enteric components. Immunohistochemically, all patients expressed at least three of the five intestinal markers: CDX2, CK20, HNF4α, MUC2, and SATB2. None of the patients expressed TTF-1 and NKX3.1. Three cases showed nuclear accumulation of β-catenin, indicating activation of the Wnt/β-catenin signaling pathway; APC mutations were detected in one of these cases. TP53 mutations were detected in three cases. Mutated EGFR or ALK fusions were not detected. Our study demonstrates that pulmonary enteric-type adenocarcinomas share immunohistochemical features and genetic alterations with colorectal adenocarcinomas, which are characterized by frequent activation of the Wnt/β-catenin signaling pathway and a lack of actionable mutations.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Data availability

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy and ethical restrictions.

References

  1. Tsao MS, Fraser RS (1991) Primary pulmonary adenocarcinoma with enteric differentiation. Cancer 68:1754–1757

    Article  CAS  PubMed  Google Scholar 

  2. Join D, MacMahon H, Nakatani Y et al (2021) Enteric-type adenocarcinoma. WHO classification of tumors series, thoracic tumors. Lyon, France, International Agency for Research on Cancer, pp 83–84

    Google Scholar 

  3. Gong J, Fan Y, Lu H (2021) Pulmonary enteric adenocarcinoma. Transl Oncol 14:101123

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Zhao L, Huang S, Liu J et al (2017) Clinicopathological, radiographic, and oncogenic features of primary pulmonary enteric adenocarcinoma in comparison with invasive adenocarcinoma in resection specimens. Medicine (Baltimore) (2017) 96:e8153

    Article  PubMed  Google Scholar 

  5. Zhang J, Xiang C, Han Y et al (2019) Differential diagnosis of pulmonary enteric adenocarcinoma and metastatic colorectal carcinoma with the assistance of next-generation sequencing and immunohistochemistry. J Cancer Res Clin Oncol 145:269–279

    Article  CAS  PubMed  Google Scholar 

  6. Liu Y, Lu T, Yuan M et al (2023) Genomic and transcriptomic insights into the precision treatment of pulmonary enteric adenocarcinoma. Lung Cancer 179:107169

    Article  CAS  PubMed  Google Scholar 

  7. Kishikawa S, Hayashi T, Saito T et al (2022) Distinct properties of pure- and mixed-type high-grade fetal lung adenocarcinomas by genetic profiling and transcription factor expression. Virchows Arch 480:609–619

    Article  CAS  PubMed  Google Scholar 

  8. Boland CR, Thibodeau SN, Hamilton SR et al (1998) A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 58:5248–5257

    CAS  PubMed  Google Scholar 

  9. Matsushima J, Yazawa T, Suzuki M et al (2017) Clinicopathological, immunohistochemical, and mutational analyses of pulmonary enteric adenocarcinoma: usefulness of SATB2 and β-catenin immunostaining for differentiation from metastatic colorectal carcinoma. Hum Pathol 64:179–185

    Article  CAS  PubMed  Google Scholar 

  10. Bian T, Zhao J, Feng J et al (2017) Combination of cadherin-17 and SATB homeobox 2 serves as potential optimal makers for the differential diagnosis of pulmonary enteric adenocarcinoma and metastatic colorectal adenocarcinoma. Oncotarget 8:63442–63452

    Article  PubMed  PubMed Central  Google Scholar 

  11. Jurmeister P, Schöler A, Arnold A et al (2019) DNA methylation profiling reliably distinguishes pulmonary enteric adenocarcinoma from metastatic colorectal cancer. Mod Pathol 2019:32:855–865

    Article  CAS  PubMed  Google Scholar 

  12. Jurmeister P, Vollbrecht C, Behnke A et al (2019) Next generation sequencing of lung adenocarcinoma subtypes with intestinal differentiation reveals distinct molecular signatures associated with histomorphology and therapeutic options. Lung Cancer 138:43–51

    Article  PubMed  Google Scholar 

  13. Xie M, Chen D, Li Y et al (2022) Genetic mutation profiles and immune microenvironment analysis of pulmonary enteric adenocarcinoma. Diagn Pathol 17:30

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Okada F, Takeda M, Fujii T et al (2022) Clinicopathological and genetic analyses of pulmonary enteric adenocarcinoma. J Clin Pathol. https://doi.org/10.1136/jcp-2022-208583

  15. Chen M, Liu P, Yan F et al (2018) Distinctive features of immunostaining and mutational load in primary pulmonary enteric adenocarcinoma: implications for differential diagnosis and immunotherapy. J Transl Med 16:81

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Skalova A, Sar A, Laco J et al (2018) The role of SATB2 as a diagnostic marker of sinonasal intestinal-type adenocarcinoma. Appl Immunohistochem Mol Morphol 26:140–146

    Article  CAS  PubMed  Google Scholar 

  17. Sjöstedt S, Schmidt AY, Vieira FG et al (2021) Major driver mutations are shared between sinonasal intestinal-type adenocarcinoma and the morphologically identical colorectal adenocarcinoma. J Cancer Res Clin Oncol 147:1019–1027

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

This work was performed in part at the Intractable Disease Research Center, Juntendo University.

Funding

This study was partly supported by grants by the Grant-in-Aid for Japan Society for the Promotion of Science (JSPS) KAKENHI (Grant Number #22K15416 and 22H02842).

Author information

Authors and Affiliations

Authors

Consortia

Contributions

Satsuki Kishikawa, Takuo Hayashi, Ayako Ura, Noriko Sasahara, Tsuyoshi Saito, and Takashi Yao provided histopathological and immunohistochemical information. Kazuya Takamochi and Kenji Suzuki provided clinical information on the patient. Satsuki Kishikawa, Takuo Hayashi, and Tsuyoshi Saito conceived the molecular experiments and analyzed the data. All authors were involved in writing the paper and provided final approval of the submitted and published versions.

Corresponding author

Correspondence to Takuo Hayashi.

Ethics declarations

Conflict of interest

The authors declare no competing interests.

Additional information

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kishikawa, S., Hayashi, T., Takamochi, K. et al. Frequent nuclear β-catenin expression in pulmonary enteric-type adenocarcinoma according to the current World Health Organization criteria. Virchows Arch 483, 699–703 (2023). https://doi.org/10.1007/s00428-023-03657-9

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00428-023-03657-9

Keywords

Navigation