SMAD4 and KCNQ3 alterations are associated with lymph node metastases in oesophageal adenocarcinoma

  • Kieran Foley
  • , David Shorthouse
  • , Eric Rahrmann
  • , Lizhe Zhuang
  • , Ginny Devonshire
  • , Richard J. Gilbertson
  • , Rebecca C. Fitzgerald
  • , Benjamin A. Hall
  • , Rebecca C. Fitzgerald
  • , Paul A.W. Edwards
  • , Nicola Grehan
  • , Barbara Nutzinger
  • , Elwira Fidziukiewicz
  • , Aisling M. Redmond
  • , Sujath Abbas
  • , Adam Freeman
  • , Elizabeth C. Smyth
  • , Maria O’Donovan
  • , Ahmad Miremadi
  • , Shalini Malhotra
  • Monika Tripathi, Calvin Cheah, Hannah Coles, Conor Flint, Matthew Eldridge, Maria Secrier, Ginny Devonshire, Sriganesh Jammula, Jim Davies, Charles Crichton, Nick Carroll, Richard H. Hardwick, Peter Safranek, Andrew Hindmarsh, Vijayendran Sujendran, Stephen J. Hayes, Yeng Ang, Andrew Sharrocks, Shaun R. Preston, Izhar Bagwan, Vicki Save, Richard J.E. Skipworth, Ted R. Hupp, J. Robert O’Neill, Olga Tucker, Andrew Beggs, Michael Scott, Richard Turkington, Damian McManus, Helen Coleman, Oesophageal Cancer Clinical and Molecular Stratification (OCCAMS) consortium

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Metastasis in oesophageal adenocarcinoma (OAC) is an important predictor of survival. Radiological staging is used to stage metastases in patients, and guide treatment selection, but is limited by the accuracy of the approach. Improvements in staging will lead to improved clinical decision making and patient outcomes. Sequencing studies on primary tumours and pre-cancerous tissue have revealed the mutational landscape of OAC, and increasingly cheap and widespread sequencing approaches offer the potential to improve staging assessment. In this work we present an analysis of lymph node metastases found by radiological and pathological sampling, identifying new roles of the genes SMAD4 and KCNQ3 in metastasis. Through transcriptomic analysis we find that both genes are associated with canonical Wnt pathway activity, but KCNQ3 is uniquely associated with changes in planar cell polaritiy associated with non-canonical Wnt signalling. We go on to validate our observations in KCNQ3 in cell line and xenograph systems, showing that overexpression of KCNQ3 reduces wound closure and the number of metastases observed. Our results suggest both genes as novel biomarkers of metastatic risk and offer new potential routes to drug targeting.

Original languageEnglish
Article number166867
JournalBiochimica et Biophysica Acta - Molecular Basis of Disease
Volume1870
Issue number1
Early online date01 Sept 2023
DOIs
Publication statusPublished - Jan 2024

Bibliographical note

Publisher Copyright:
© 2023

Keywords

  • Imaging
  • Metastasis
  • Mutation
  • Oesophageal adenocarcinoma
  • Radiology
  • Wnt Signalling

ASJC Scopus subject areas

  • Molecular Medicine
  • Molecular Biology

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