Gallbladder adenocarcinomas undergo subclonal diversification and selection from precancerous lesions to metastatic tumors

Elife. 2022 Dec 8:11:e78636. doi: 10.7554/eLife.78636.

Abstract

We aimed to elucidate the evolutionary trajectories of gallbladder adenocarcinoma (GBAC) using multi-regional and longitudinal tumor samples. Using whole-exome sequencing data, we constructed phylogenetic trees in each patient and analyzed mutational signatures. A total of 11 patients including 2 rapid autopsy cases were enrolled. The most frequently altered gene in primary tumors was ERBB2 and TP53 (54.5%), followed by FBXW7 (27.3%). Most mutations in frequently altered genes in primary tumors were detectable in concurrent precancerous lesions (biliary intraepithelial neoplasia [BilIN]), but a substantial proportion was subclonal. Subclonal diversity was common in BilIN (n=4). However, among subclones in BilIN, a certain subclone commonly shrank in concurrent primary tumors. In addition, selected subclones underwent linear and branching evolution, maintaining subclonal diversity. Combined analysis with metastatic tumors (n=11) identified branching evolution in nine patients (81.8%). Of these, eight patients (88.9%) had a total of 11 subclones expanded at least sevenfold during metastasis. These subclones harbored putative metastasis-driving mutations in cancer-related genes such as SMAD4, ROBO1, and DICER1. In mutational signature analysis, six mutational signatures were identified: 1, 3, 7, 13, 22, and 24 (cosine similarity >0.9). Signatures 1 (age) and 13 (APOBEC) decreased during metastasis while signatures 22 (aristolochic acid) and 24 (aflatoxin) were relatively highlighted. Subclonal diversity arose early in precancerous lesions and clonal selection was a common event during malignant transformation in GBAC. However, selected cancer clones continued to evolve and thus maintained subclonal diversity in metastatic tumors.

Keywords: cancer biology; carcinogenesis; clonal evolution; gallbladder adenocarcinoma; genetics; genomics; human; metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma* / genetics
  • Adolescent
  • Bile Pigments
  • DEAD-box RNA Helicases
  • Gallbladder
  • Humans
  • Mutation
  • Nerve Tissue Proteins
  • Phylogeny
  • Precancerous Conditions* / genetics
  • Receptors, Immunologic
  • Ribonuclease III

Substances

  • Nerve Tissue Proteins
  • Receptors, Immunologic
  • Bile Pigments
  • DICER1 protein, human
  • Ribonuclease III
  • DEAD-box RNA Helicases

Associated data

  • SRA/PRJNA821382

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.