Evidence map›Paper›PMID 40130316›Full record

ArticleCancer medicine2025

Daxx Variation as a Potential Predictive Marker of the Therapeutic Response to Neoadjuvant Chemoradiotherapy in Locally Advanced Rectal Cancer.

Xi Zhu, Xiaoming Kao, Leilei Liu, Xuan Wang, Yang Li, Qiurong Li

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Article in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Xi ZhuResearch Institute of General Surgery, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.ORCID https://orcid.org/0000-0001-9193-4711
Xiaoming KaoResearch Institute of General Surgery, Jinling Hospital, Nanjing Medical University, Nanjing, China.
Leilei LiuDepartment of Pathology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Xuan WangDepartment of Pathology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Yang LiResearch Institute of General Surgery, Jinling Hospital, Nanjing Medical University, Nanjing, China.
Qiurong LiResearch Institute of General Surgery, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe response to neoadjuvant chemoradiotherapy (NACRT) for locally advanced rectal cancer (LARC) varies from achieving a complete pathological response to encountering resistance to treatment. Therefore, biomarkers for predicting the NACRT responses should be identified. This prospective study aimed to identify key genomic biomarkers as the predictors of the NACRT response with LARC.

methodsOverall, 67 patients with LARC treated with NACRT and proctectomy were divided into two groups based on the tumor regression grade (TRG) for identifying key biomarkers. Patients with a TRG of 0 or 1 were assigned to the sensitive response group, and patients with a TRG of 2 or 3 were the resistant response group. Twenty-nine postsurgical tumor samples were collected for whole exome sequencing (WES) to identify genomic variation biomarkers. The other 38 pairs of tumor specimens from pretreatment and postsurgery samples were evaluated by immunohistochemistry (IHC) to examine the biomarker features.

resultsIn the WES subcohort, 11 genes showed copy number variation, including FNKBIA, ARID1A, CCND2, CDK4, LYN, MDM2, RAD51B, RARA, SPEN, STAT3, and Daxx, which has the highest copy number variation. For the IHC subcohort, Daxx was initially highly expressed in the nuclei of tumor cells, particularly in the sensitive response group, while varying its expression after NACRT, demonstrating that Daxx levels were related to treatment responses and the survival benefit, especially a better disease-free survival (DFS).

conclusionWe identified multiple genomic variations between sensitive and resistant responders and verified that Daxx is a potential predictive biomarker of the response to NACRT in LARC.

Indexed as

Biomarkers, TumorCo-Repressor ProteinsMolecular ChaperonesRectal NeoplasmsAdultAgedChemoradiotherapyChemoradiotherapy, AdjuvantDNA Copy Number VariationsExome SequencingFemaleHumansMaleMiddle AgedNeoadjuvant TherapyPrognosisBiomarkers, TumorCo-Repressor ProteinsDAXX protein, humanMolecular ChaperonesDaxxlocally advanced rectal cancerneoadjuvant chemoradiotherapypredictive biomarkertherapeutic response

Identifiers

PMID40130316
PMCPMC11933753

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