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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 42 Issue 5
May  2026
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Article Contents

Expression levels of Yes-associated protein 1 and human collagen type Ⅵ alpha 1 in pancreatic cancer under hyperglycemic conditions and their impact on prognosis

DOI: 10.12449/JCH260519
Research funding:

National Natural Science Foundation of China (81860508)

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  • Corresponding author: QIN Wen, fenglingcao1980@163.com (ORCID: 0009-0002-8282-7388)
  • Received Date: 2025-12-01
  • Accepted Date: 2026-03-02
  • Published Date: 2026-05-25
  •   Objective  To investigate the changes in the expression levels of Yes-associated protein 1 (YAP1) and human collagen type Ⅵ alpha 1 (COL6A1) in pancreatic cancer under hyperglycemic conditions and their association with prognosis.  Methods  GEPIA database and R software were used to analyze the expression levels of YAP1 and COL6A1 and their correlation in pancreatic cancer, as well as their impact on the prognosis of patients with pancreatic cancer. The cBioPortal database was used to identify the co-expressed genes of YAP1 and COL6A1 in pancreatic cancer, and the gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses were performed. Quantitative real-time PCR and Western blot were used to measure the mRNA and protein expression levels of YAP1 and COL6A1 in human pancreatic cancer PANC-1 cells cultured under hyperglycemic or normoglycemic conditions. A nude mouse model of pancreatic cancer with type 2 diabetes was established, and immunohistochemistry was used to measure the expression of YAP1 and COL6A1 in subcutaneous tumor tissue. Clinical specimens and data of 96 patients with pancreatic cancer were collected from January 2016 to January 2020 in the First Affiliated Hospital of Guangxi Medical University, Guangxi Medical University Cancer Hospital and Wuming Hospital Affiliated to Guangxi Medical University. Among them, 48 patients with pancreatic cancer and diabetes were enrolled as study group, and 48 patients with pancreatic cancer alone were enrolled as control group; immunohistochemistry was used to measure the expression levels of YAP1 and COL6A1 in tissue samples from both groups, and their association with clinical indicators and survival outcomes was analyzed. The t-test was used for comparison of continuous data between groups, and the chi-square test or the Mann-Whitney U test was used for comparison of categorical data between groups; the Pearson correlation analysis was used for normally distributed continuous variables, while the Spearman correlation analysis was used for discontinuous variables or non-normally distributed variables. The Kaplan-Meier method was used to plot survival curves, and the Log-rank test was used for comparison of survival rates. The Cox proportional hazards model was used to perform univariate and multivariate analyses.  Results  Both YAP1 and COL6A1 were highly expressed in pancreatic cancer, with a strong correlation between them (r=0.85, P<0.001), and they were associated with the poor prognosis of patients (hazard ratio [HR]=1.8 and 1.5, both P<0.05). YAP1 and COL6A1 were significantly correlated with 219 and 122 genes, respectively (r=0.83 and 0.86, both P<0.05), and the GO and KEGG enrichment analyses showed that these genes affected the development and progression of pancreatic cancer through extracellular matrix-receptor interaction, the Hippo signaling pathway, and the phosphatidylinositol 3-kinase/protein kinase B signaling pathway. Quantitative real-time PCR and Western blot showed that there were significant increases in the mRNA and protein expression levels of YAP1 and COL6A1 in human pancreatic cancer PANC-1 cells under hyperglycemic conditions (mRNA expression: t=4.726 and 6.197, both P<0.05; protein expression: t=6.826 and 5.254, both P<0.05). Immunohistochemistry showed that there were significant increases in the expression levels of YAP1 and COL6A1 in subcutaneous tumor tissue of nude mice, with a positive correlation between them (r=0.985, P<0.001). For the clinical specimens of pancreatic cancer tissue, immunohistochemistry showed that there were significant increases in the positive expression levels of YAP1 and COL6A1 proteins in the study group, with a positive correlation between them (r=0.882, P<0.001). The multivariate analysis of clinical data showed that lymph node metastasis (HR=0.083, 95% confidence interval [CI]: 0.030 — 0.231, P<0.05), distant organ metastasis (HR=0.166, 95%CI: 0.065 — 0.420, P<0.05), YAP1 expression level (HR=2.027, 95%CI: 1.065 — 3.857, P<0.05), and COL6A1 expression level (HR=2.044, 95%CI: 1.019 — 4.099, P<0.05) were independent influencing factors for the prognosis of patients with pancreatic cancer. The survival analysis showed that the high YAP1 expression group had a significantly lower 2-year survival rate than the low YAP1 expression group (6.82% vs 25.00%, χ2=16.382, P<0.001), and the high COL6A1 expression group had a significantly lower 2-year survival rate than the low COL6A1 expression group (14.58% vs 18.75%, χ2=4.579, P=0.032).  Conclusion  The hyperglycemic environment promotes the high expression of YAP1 and COL6A1 in pancreatic cancer, which is associated with poor prognosis in patients.

     

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  • [1]
    CHEN SM, PHUC PT, NGUYEN PA, et al. A novel prediction model of the risk of pancreatic cancer among diabetes patients using multiple clinical data and machine learning[J]. Cancer Med, 2023, 12( 19): 19987- 19999. DOI: 10.1002/cam4.6547.
    [2]
    QIN C, LI TY, LIN C, et al. The systematic role of pancreatic cancer exosomes: Distant communication, liquid biopsy and future therapy[J]. Cancer Cell Int, 2024, 24( 1): 264. DOI: 10.1186/s12935-024-03456-5.
    [3]
    WANG C, LYU J, MA YL. Analysis of the clinical characteristics and prognostic risk factors in 100 patients with pancreatic cancer[J]. J Clin Exp Med, 2025, 24( 23): 2510- 2514. DOI: 10.3969/j.issn.1671-4695.2025.23.013.

    王琛, 吕婧, 马于丽. 胰腺癌100例患者临床特征及预后的危险因素分析[J]. 临床和实验医学杂志, 2025, 24( 23): 2510- 2514. DOI: 10.3969/j.issn.1671-4695.2025.23.013.
    [4]
    ANDERSEN DK, KORC M, PETERSEN GM, et al. Diabetes, pancreatogenic diabetes, and pancreatic cancer[J]. Diabetes, 2017, 66( 5): 1103- 1110. DOI: 10.2337/db16-1477.
    [5]
    LEGA IC, LIPSCOMBE LL. Review: Diabetes, obesity, and cancer-pathophysiology and clinical implications[J]. Endocr Rev, 2020, 41( 1): bnz014. DOI: 10.1210/endrev/bnz014.
    [6]
    RENEHAN AG, TIPPING O, WANG MY. Diabetes and cancer: Doubts of a causal link[J]. Int J Cancer, 2024, 154( 11): 1875- 1876. DOI: 10.1002/ijc.34862.
    [7]
    COSMIN STAN M, PAUL D. Diabetes and cancer: A twisted bond[J]. Oncol Rev, 2024, 18: 1354549. DOI: 10.3389/or.2024.1354549.
    [8]
    KHAN I, KAMAL A, AKHTAR S. Diabetes driven oncogenesis and anticancer potential of repurposed antidiabetic drug: A systemic review[J]. Cell Biochem Biophys, 2024, 82( 3): 1907- 1929. DOI: 10.1007/s12013-024-01387-6.
    [9]
    PLISZKA M, SZABLEWSKI L. Associations between diabetes mellitus and selected cancers[J]. Int J Mol Sci, 2024, 25( 13): 7476. DOI: 10.3390/ijms25137476.
    [10]
    CHEN JC, WANG XY, HE Q, et al. YAP activation in renal proximal tubule cells drives diabetic renal interstitial fibrogenesis[J]. Diabetes, 2020, 69( 11): 2446- 2457. DOI: 10.2337/db20-0579.
    [11]
    LI S, ZHU H, CHEN HD, et al. Glucose promotes epithelial-mesenchymal transitions in bladder cancer by regulating the functions of YAP1 and TAZ[J]. J Cell Mol Med, 2020, 24( 18): 10391- 10401. DOI: 10.1111/jcmm.15653.
    [12]
    ZHANG Y, LIU ZY, YANG X, et al. H3K27 acetylation activated-COL6A1 promotes osteosarcoma lung metastasis by repressing STAT1 and activating pulmonary cancer-associated fibroblasts[J]. Theranostics, 2021, 11( 3): 1473- 1492. DOI: 10.7150/thno.51245.
    [13]
    ZHANG X, QIAO YX, WU Q, et al. The essential role of YAP O-GlcNAcylation in high-glucose-stimulated liver tumorigenesis[J]. Nat Commun, 2017, 8: 15280. DOI: 10.1038/ncomms15280.
    [14]
    ORTILLON J, LE BAIL JC, VILLARD E, et al. High glucose activates YAP signaling to promote vascular inflammation[J]. Front Physiol, 2021, 12: 665994. DOI: 10.3389/fphys.2021.665994.
    [15]
    YU Q, ZHANG Z, ZHANG HJ. Effect of glucose variability on pancreatic cancer through regulation of COL6A1[J]. Cancer Manag Res, 2021, 13: 1291- 1298. DOI: 10.2147/CMAR.S293473.
    [16]
    XU YN, HUANG XH, TANG ZP, et al. Establishment and in vivo imaging observation of a nude mouse model of type 2 diabetes mellitus and pancreatic cancer[J]. J Clin Hepatol, 2024, 40( 6): 1231- 1239. DOI: 10.12449/JCH240625.

    许永宁, 黄雪桓, 唐芷盼, 等. 2型糖尿病胰腺癌裸鼠模型的建立及活体成像观察[J]. 临床肝胆病杂志, 2024, 40( 6): 1231- 1239. DOI: 10.12449/JCH240625.
    [17]
    LIU JW, XU L, ZHAN XR. LncRNA MALAT1 regulates diabetic cardiac fibroblasts through the Hippo-YAP signaling pathway[J]. Biochem Cell Biol, 2020, 98( 5): 537- 547. DOI: 10.1139/bcb-2019-0434.
    [18]
    WANG Y, XU JM, CHENG ZF. YAP1 promotes high glucose-induced inflammation and extracellular matrix deposition in glomerular mesangial cells by modulating NF-κB/JMJD3 pathway[J]. Exp Ther Med, 2021, 22( 6): 1349. DOI: 10.3892/etm.2021.10784.
    [19]
    BERTERO T, OLDHAM WM, GRASSET EM, et al. Tumor-stroma mechanics coordinate amino acid availability to sustain tumor growth and malignancy[J]. Cell Metab, 2019, 29( 1): 124- 140.e10. DOI: 10.1016/j.cmet.2018.09.012.
    [20]
    ZHANG TC, CHEN JJ, YANG H, et al. Stromal softness confines pancreatic cancer growth through lysosomal-cathepsin mediated YAP1 degradation[J]. Cell Mol Life Sci, 2024, 81( 1): 442. DOI: 10.1007/s00018-024-05466-y.
    [21]
    BUGLIO G LO, CICERO A LO, CAMPORA S, et al. The multifaced role of collagen in cancer development and progression[J]. Int J Mol Sci, 2024, 25( 24): 13523. DOI: 10.3390/ijms252413523.
    [22]
    CHEN YZ, ZHAO XG, SUN J, et al. YAP1/Twist promotes fibroblast activation and lung fibrosis that conferred by miR-15a loss in IPF[J]. Cell Death Differ, 2019, 26( 9): 1832- 1844. DOI: 10.1038/s41418-018-0250-0.
    [23]
    ZHANG YL, LIU QP, NING J, et al. The proteasome-dependent degradation of ALKBH5 regulates ECM deposition in PM2.5 exposure-induced pulmonary fibrosis of mice[J]. J Hazard Mater, 2022, 432: 128655. DOI: 10.1016/j.jhazmat.2022.128655.
    [24]
    YE S, LIU Y, FULLER AM, et al. TGFβ and Hippo pathways cooperate to enhance sarcomagenesis and metastasis through the hyaluronan-mediated motility receptor(HMMR)[J]. Mol Cancer Res, 2020, 18( 4): 560- 573. DOI: 10.1158/1541-7786.MCR-19-0877.
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