# Characterization of neocentromeric marker chromosome derived from chromosome 11: a rare entity in four patients with acute leukemia

**Authors:** Iveta Mendlikova, Jana Brezinova, Karla Svobodova, Lenka Pavlistova, Marie Valerianova, Jan Valka, Marketa Markova Stastna, Anna Jonasova, Zuzana Zemanova, Sarka Ransdorfova

PMC · DOI: 10.1007/s10577-026-09798-2 · Chromosome Research · 2026-03-26

## TL;DR

This study reports four rare cases of neocentromeres on chromosome 11 in patients with acute leukemia, highlighting their potential role in genomic instability and poor outcomes.

## Contribution

First report of neocentromeres derived from chromosome 11 in acute leukemia, linking them to disease progression and genomic instability.

## Key findings

- Four patients (3.5%) had neocentromeres on derivative chromosome 11 in acute leukemia.
- All four patients had complex karyotypes and died, indicating poor prognosis.
- Neocentromeres may contribute to genomic instability and aggressive disease progression.

## Abstract

Neocentromeres are newly formed chromosomal regions that can replace the function of traditional centromeres and are well documented in human clinical studies. However, their occurrence in neoplasia, including acute leukemia, appears to be rare. We analyzed complex karyotypes in bone marrow cells from 113 patients with acute myeloid leukemia and one patient with acute lymphoblastic leukemia using centromeric/multicentromeric fluorescence in situ hybridization and identified four cases (3.5%) with derivative chromosomes exhibiting newly formed constrictions. Three of these patients had secondary leukemia following preexisting hematological disorders, suggesting a potential role for neocentromeres in disease progression. In all four cases, neocentromeres were detected on derivative chromosome 11. To our knowledge, this is the first report of neocentromeres derived from this chromosome in acute leukemia. All four patients in our study died; however, all exhibited complex karyotypes, which are independently associated with poor prognosis and an aggressive disease course. Neocentromeres are a rare but potentially important source of genomic instability in malignant diseases. Generally, the formation of a new constriction allows mitotic rescue of acentric chromosomes, preventing their loss. An increase in genomic alterations in tumor cells predicts a more aggressive disease course and adverse outcomes. Due to limited data, the prognostic significance of neocentromeres remains unclear. Further rigorous investigation is required to deepen our understanding of the mechanisms underlying neocentromere formation and their implications in cancer.

## Linked entities

- **Diseases:** acute myeloid leukemia (MONDO:0015667), acute lymphoblastic leukemia (MONDO:0004967), acute leukemia (MONDO:0010643)

## Full-text entities

- **Genes:** KMT2A (lysine methyltransferase 2A) [NCBI Gene 4297] {aka ALL-1, ALL1, CXXC7, GAS7, HRX, HTRX}, CNTRL (centriolin) [NCBI Gene 11064] {aka CEP1, CEP110, FAN, bA165P4.1}
- **Diseases:** lung carcinoma (MESH:D008175), died (MESH:D003643), FL (MESH:D008224), Cancer (MESH:D009369), leukemia (MESH:D007938), AML (MESH:D015470), chromosomal abnormalities (MESH:D002869), chronic myelomonocytic leukemia (MESH:D015477), myelodysplastic syndrome (MESH:D009190), Hematological malignancies (MESH:D019337), hematologic disease (MESH:D006402), acute lymphoblastic leukemia (MESH:D054198), MDS RAEB-2 (MESH:D000754), dysplasia (MESH:D015792), aneuploidy (MESH:D000782), T-cell non-Hodgkin lymphoma (MESH:D008228)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** NA12878 — Homo sapiens (Human), Transformed cell line (CVCL_7526)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13021727/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13021727/full.md

---
Source: https://tomesphere.com/paper/PMC13021727