# Association of NUDT17 rs9286836 and rs2004659 variants with breast cancer risk in Bangladeshi Women

**Authors:** Md. Shajid Hossain Rafi, Md. Shalahuddin Millat, Md Abdul Barek, Syed Masudur Rahman Dewan, Mohammad Shahriar, Zabun Nahar, Mohammad Safiqul Islam, Milad Khorasani, Milad Khorasani, Milad Khorasani

PMC · DOI: 10.1371/journal.pone.0344584 · PLOS One · 2026-03-19

## TL;DR

This study explores how two genetic variants in the NUDT17 gene are linked to breast cancer risk in Bangladeshi women.

## Contribution

The study identifies a protective effect of the NUDT17 rs2004659 variant against breast cancer in a South Asian population.

## Key findings

- The rs2004659 variant showed a protective association with breast cancer, especially in heterozygous individuals.
- The AA haplotype increased breast cancer risk, while AG and GA haplotypes reduced it.
- NUDT17 expression was higher in cancer tissues and influenced by the genetic variants.

## Abstract

Breast cancer is a multifaceted illness impacted by genetic factors as well as environmental influences. While variants in the NUDT17 gene have been associated with cancer biology, their involvement in breast cancer is still inadequately investigated, especially within South Asian populations. This study investigated the association between two NUDT17 polymorphisms, rs9286836 and rs2004659, and breast cancer risk in Bangladeshi women using a case–control design. A total of 240 breast cancer patients and 240 age-, sex-, and BMI-matched healthy controls were enrolled. Genomic DNA was extracted from blood samples, and genotyping was performed using tetra-primer ARMS-PCR for rs9286836 and PCR–RFLP for rs2004659. The statistical methods employed included chi-square tests for genotype distributions and logistic regression to calculate odds ratios (ORs) with 95% confidence intervals (CIs). Genotyping for NUDT17 rs9286836 was successfully completed for all recruited participants. However, for rs2004659, high-quality genotyping data were available for 204 breast cancer cases and 204 controls after quality control procedures. No significant association was observed between rs9286836 and breast cancer risk across the tested genetic models. In contrast, rs2004659 showed a robust protective association with breast cancer, particularly among heterozygous individuals, and this protective effect was consistently observed across the dominant, over-dominant, and allelic models. Haplotype analysis revealed that the AA haplotype was associated with an increased risk of breast cancer, whereas the AG and GA haplotypes were associated with a reduced risk. Expression analysis further demonstrated elevated NUDT17 levels in breast cancer tissues and genotype-dependent expression effects for both variants. These findings suggest a protective role of rs2004659 in breast cancer susceptibility and highlight the potential of NUDT17 polymorphisms as biomarkers in Bangladeshi women.

## Linked entities

- **Genes:** NUDT17 (nudix hydrolase 17) [NCBI Gene 200035]
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** NUDT21 (nudix hydrolase 21) [NCBI Gene 11051] {aka CFIM25, CPSF5}, NUDT5 (nudix hydrolase 5) [NCBI Gene 11164] {aka YSA1, YSA1H, YSAH1, hNUDT5}, NUDT2 (nudix hydrolase 2) [NCBI Gene 318] {aka APAH1, IDDPN}, VDR (vitamin D receptor) [NCBI Gene 7421] {aka NR1I1, PPP1R163}, BARD1 (BRCA1 associated RING domain 1) [NCBI Gene 580], NUDT10 (nudix hydrolase 10) [NCBI Gene 170685] {aka APS2, DIPP3-alpha, DIPP3a}, MAP3K1 (mitogen-activated protein kinase kinase kinase 1) [NCBI Gene 4214] {aka MAPKKK1, MEKK, MEKK 1, MEKK1, SRXY6}, NUDT15 (nudix hydrolase 15) [NCBI Gene 55270] {aka MTH2, NUDT15D}, ERCC2 (ERCC excision repair 2, TFIIH core complex helicase subunit) [NCBI Gene 2068] {aka COFS2, CXPD, EM9, TFIIH, TTD, TTD1}, NUDT1 (nudix hydrolase 1) [NCBI Gene 4521] {aka MTH1}, NUDT17 (nudix hydrolase 17) [NCBI Gene 200035], PALB2 (partner and localizer of BRCA2) [NCBI Gene 79728] {aka BROVCA5, FANCN, PNCA3}
- **Diseases:** oral squamous cell carcinoma (MESH:D000077195), colorectal cancer (MESH:D015179), Breast (MESH:D061325), inflammatory diseases (MESH:D007249), Breast Cancer (MESH:D001943), gastric cancer (MESH:D013274), ccRCC (MESH:D002292), underweight (MESH:D013851), DCIS (MESH:D002285), medullary carcinoma (MESH:D018276), metastasis (MESH:D009362), deaths (MESH:D003643), carcinogenesis (MESH:D063646), Cancer (MESH:D009369), obesity (MESH:D009765), nodal (MESH:D013611), invasive ductal carcinoma (MESH:D044584), invasive lobular carcinoma (MESH:D018275)
- **Chemicals:** EDTA (MESH:D004492), nucleotide (MESH:D009711), Vitamin D (MESH:D014807), polyphosphates (MESH:D011122), agarose (MESH:D012685), ethidium bromide (MESH:D004996), NTPs (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs2004659, rs9286836, rs10910830, rs2276466, rs249954, rs152451, rs13181, rs10910829

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC13001948/full.md

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Source: https://tomesphere.com/paper/PMC13001948