﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Maad Rayan Publishing Company</PublisherName>
      <JournalTitle>Biomedicine Advances</JournalTitle>
      <Issn>3080-0382</Issn>
      <Volume>3</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2026</Year>
        <Month>04</Month>
        <DAY>27</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Vitamin D and hematologic malignancies: A comprehensive review of its role in therapeutic potential, pathogenesis, and prognosis</ArticleTitle>
    <FirstPage>64</FirstPage>
    <LastPage>71</LastPage>
    <ELocationID EIdType="doi">10.34172/bma.63</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Abolfazl</FirstName>
        <LastName>Jalilvand</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0006-1284-1626</Identifier>
      </Author>
      <Author>
        <FirstName>Mohammadhossein</FirstName>
        <LastName>Kouhpaeenejad</LastName>
      </Author>
      <Author>
        <FirstName>Leila</FirstName>
        <LastName>Faeli</LastName>
      </Author>
      <Author>
        <FirstName>Nesa</FirstName>
        <LastName>Rashidi</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0005-4293-8050</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>REVIEW</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/bma.63</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>12</Month>
        <Day>22</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2026</Year>
        <Month>03</Month>
        <Day>19</Day>
      </PubDate>
    </History>
    <Abstract>Vitamin D has immunomodulatory, anti-proliferative, and pro-differentiative effects that are increasingly linked to hematologic malignancies, beyond its traditional function in maintaining calcium-phosphate balance. Patients with leukemia and lymphoma frequently have vitamin D deficiency, which has been linked to poor prognostic characteristics and a lower chance of survival. The active metabolite 1,25-dihydroxyvitamin D3 stimulates cellular differentiation, suppresses proliferation, and triggers apoptosis in acute leukemias (ALL and AML) by means of vitamin D receptor (VDR)-mediated transcriptional regulation. Based on empirical evidence, a higher tumor burden, a worse response to treatment, and an advanced disease stage are all associated with low vitamin D levels in chronic leukemias (CLL and CML). Similarly, hypovitaminosis D has been associated with worse treatment outcomes for both Hodgkin and non-Hodgkin lymphomas. By modifying cytokine production, immune cell function, angiogenesis, cell cycle regulation, and tumor–microenvironment interactions, vitamin D mechanistically affects leukemogenesis and lymphomagenesis. This review outlines the most recent molecular and clinical data that suggests vitamin D may be used as a prognostic biomarker and an adjuvant therapeutic target in hematologic malignancies. However, to elucidate its therapeutic impact and clinical utility, extensive prospective and randomized studies are needed. </Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Vitamin D</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Malignancy</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Biomarker</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Diagnosis</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Prognosis</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>