<?xml version="1.1" encoding="utf-8"?>
<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">OTD</journal-id><journal-title-group><journal-title>Oncology Treatment Discovery</journal-title></journal-title-group><issn>3083-4996</issn><eissn>2981-8079</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/otd.v4i1.14270</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Research Progress of Mir143 in Tumors and Its Guiding Significance in Lung Cancer Research</title><url>https://artdesignp.com/journal/OTD/4/1/10.26689/otd.v4i1.14270</url><author>TongChengbi,QiJi,ZhuYaxing,YuYang,JiaTianhong</author><pub-date pub-type="publication-year"><year>2026</year></pub-date><volume>4</volume><issue>1</issue><history><date date-type="pub"><published-time>2026-03-18</published-time></date></history><abstract>MicroRNA-143 (miR-143) is a non-coding RNA molecule that plays a critical regulatory role in various biological processes, including cell proliferation, differentiation, and apoptosis. This review summarizes the structural characteristics of miR-143 and its expression patterns in different tumor types, with a particular focus on cervical cancer, colon cancer, and lung cancer. In most malignancies, miR-143 is downregulated and functions as a tumor suppressor by targeting oncogenes and modulating key signaling pathways. However, emerging evidence suggests that miR-143 may exhibit dual roles depending on the tumor context, as seen in certain lung cancer studies where its elevated expression correlates with poor prognosis. The interaction between miR-143 and long non-coding RNAs (lncRNAs) further expands its regulatory network and highlights its potential as a diagnostic biomarker and therapeutic target. A deeper understanding of miR-143’s multifaceted functions may offer new insights into tumor biology and treatment strategies.</abstract><keywords/></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>Xie F, Li C, Zhang X, Peng W, Wen T, 2019, MiR-143-3p Suppresses Tumorigenesis in Pancreatic Ductal Adenocarcinoma by Targeting KRAS. Biomed Pharmacother, 119: 109424.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B2" content-type="article"><label>2</label><element-citation publication-type="journal"><p>Pinweha P, Phillips CA, Gregory PA, et al., 2019, MicroRNA-143-3p Targets Pyruvate Carboxylase Expression and Controls Proliferation and Migration of DA-MB-231 Cells. Arch Biochem Biophys, 677: 108169.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B3" content-type="article"><label>3</label><element-citation publication-type="journal"><p>Baron BW, Pytel P, 2017, Expression Pattern of the BCL6 and ITM2B Proteins in Normal Human Brains and in Alzheimer Disease. Appl Immunohistochem Mol Morphol, 25(7): 489–496.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B4" content-type="article"><label>4</label><element-citation publication-type="journal"><p>Maryam N, Alihossein S, Majid K, et al., 2018, Adipose Tissue miRNA Level Variation Through Conjugated Linoleic Acid Supplementation in Diet-Induced Obese Rats. Adv Clin Exp Med, 27(11): 1477–1482.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B5" content-type="article"><label>5</label><element-citation publication-type="journal"><p>Lin XT, Zheng XB, Fan DJ, et al., 2018, MicroRNA-143 Targets ATG2B to Inhibit Autophagy and Increase Inflammatory Responses in Crohn’s Disease. Inflamm Bowel Dis, 24(4): 781–791.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B6" content-type="article"><label>6</label><element-citation publication-type="journal"><p>He Z, Yi J, Liu X, et al., 2016, MiR-143-3p Functions as a Tumor Suppressor by Regulating Cell Proliferation, Invasion and Epithelial-Mesenchymal Transition by Targeting QKI-5 in Esophageal Squamous Cell Carcinoma. Mol Cancer, 15(1): 51.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B7" content-type="article"><label>7</label><element-citation publication-type="journal"><p>Zheng X, Ge Y, Gan J, Jin Y, Cui Y, Wu Y, Liu Z, Sun G, 2025, Targeting miR-197-3p to Regulate the Proliferation and Metastasis of Esophageal Squamous Cell Carcinoma. China Pharmacological Bulletin, 41(5): 888–898.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B8" content-type="article"><label>8</label><element-citation publication-type="journal"><p>Xia C, Yang Y, Kong F, et al., 2018, MiR-143-3p Inhibits the Proliferation, Cell Migration and Invasion of Human Breast Cancer Cells by Modulating the Expression of MAPK7. Biochimie, 147: 98–104.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B9" content-type="article"><label>9</label><element-citation publication-type="journal"><p>Luo LL, Wang M, Li XP, et al., 2020, A Novel Mechanism by Which ACTA2-AS1 Promotes Cervical Cancer Progression: Acting as a ceRNA of miR-143-3p to Regulate SMAD3 Expression. Cancer Cell Int, 20: 372.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B10" content-type="article"><label>10</label><element-citation publication-type="journal"><p>Liu L, Yu X, Guo X, et al., 2012, miR-143 Is Downregulated in Cervical Cancer and Promotes Apoptosis and Inhibits Tumor Formation by Targeting Bcl-2. Mol Med Rep, 5(3): 753–760.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B11" content-type="article"><label>11</label><element-citation publication-type="journal"><p>Zhao Y, Liu X, Lu YX, 2017, MicroRNA-143 Regulates the Proliferation and Apoptosis of Cervical Cancer Cells by Targeting HIF-1α. Eur Rev Med Pharmacol Sci, 21(24): 5580–5586.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B12" content-type="article"><label>12</label><element-citation publication-type="journal"><p>Liu Z, Hu K, et al., 2022, lncRNA ACTA2-AS1 Inhibits Malignant Phenotypes of Gastric Cancer Cells. Open Med, 17(1): 266–279.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B13" content-type="article"><label>13</label><element-citation publication-type="journal"><p>Michael MZ, SM OC, van Holst Pellekaan NG, et al., 2003, Reduced Accumulation of Specific MicroRNAs in Colorectal Neoplasia. Mol Cancer Res, 1(12): 882–891.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B14" content-type="article"><label>14</label><element-citation publication-type="journal"><p>Borralho PM, Simões AE, Gomes SE, et al., 2011, miR-143 Overexpression Impairs Growth of Human Colon Carcinoma Xenografts in Mice with Induction of Apoptosis and Inhibition of Proliferation. PLoS One, 6(8): e23787.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B15" content-type="article"><label>15</label><element-citation publication-type="journal"><p>Akao Y, Nakagawa Y, Naoe T, 2006, MicroRNAs 143 and 145 Are Possible Common Onco-microRNAs in Human Cancers. Oncol Rep, 16(4): 845–850.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B16" content-type="article"><label>16</label><element-citation publication-type="journal"><p>Su J, Liang H, Yao W, et al., 2014, MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer. PLoS One, 9(12): e114420.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B17" content-type="article"><label>17</label><element-citation publication-type="journal"><p>Eckstein N, Servan K, Hildebrandt B, et al., 2009, Hyperactivation of the Insulin-Like Growth Factor Receptor I Signaling Pathway Is an Essential Event for Cisplatin Resistance of Ovarian Cancer Cells. Cancer Res, 69(7): 2996–3003.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B18" content-type="article"><label>18</label><element-citation publication-type="journal"><p>Slaby O, Svoboda M, Fabian P, et al., 2007, Altered Expression of miR-21, miR-31, miR-143 and miR-145 Is Related to Clinicopathologic Features of Colorectal Cancer. Oncology, 72(5–6): 397–402.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B19" content-type="article"><label>19</label><element-citation publication-type="journal"><p>Borralho PM, Kren BT, Castro RE, et al., 2009, MicroRNA-143 Reduces Viability and Increases Sensitivity to 5-Fluorouracil in HCT116 Human Colorectal Cancer Cells. FEBS J, 276(22): 6689–6700.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B20" content-type="article"><label>20</label><element-citation publication-type="journal"><p>Zhang XY, Wang LF, 2017, Differential Expression of miR-143 in Colorectal Cancer Tissues and Its Effects on Apoptosis and Migration of Colorectal Cancer Cells. Journal of Shanghai Jiao Tong University (Medical Edition), 37(3): 325–329.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B21" content-type="article"><label>21</label><element-citation publication-type="journal"><p>Nakajima G, Hayashi K, Xi Y, et al., 2006, Non-Coding MicroRNAs hsa-let-7g and hsa-miR-181b Are Associated with Chemoresponse to S-1 in Colon Cancer. Cancer Genomics Proteomics, 3(5): 317–324.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B22" content-type="article"><label>22</label><element-citation publication-type="journal"><p>Zhang HB, Sun LC, Ling L, et al., 2016, miR-143 Suppresses the Proliferation of NSCLC Cells by Inhibiting the Epidermal Growth Factor Receptor. Exp Ther Med, 12(3): 1795–1802.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B23" content-type="article"><label>23</label><element-citation publication-type="journal"><p>Li T, Wang B, Yuan C, et al., 2020, Correlation Analysis of miR-143 with Serum Tumor Markers and Clinical Efficacy/Prognosis in Lung Cancer Patients. Journal of Guangxi Medical University, 37(7): 1276–1282.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B24" content-type="article"><label>24</label><element-citation publication-type="journal"><p>Yu JR, Jiang R, Feng L, et al., 2022, Expression of miR-143 in Peripheral Blood of Lewis Lung Cancer Mice and Its Effect on Th1/Th2 Balance. Journal of Immunology, 38(5): 438–444.</p><pub-id pub-id-type="doi"/></element-citation></ref></ref-list></back></article>
