Screening ferroptosis related genes influencing prognosis of colon cancer through bioinformatics analysis

LI Xiao-jun ZHANG Ya-min

Acta Anatomica Sinica ›› 2023, Vol. 54 ›› Issue (4) : 445-452.

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Acta Anatomica Sinica ›› 2023, Vol. 54 ›› Issue (4) : 445-452. DOI: 10.16098/j.issn.0529-1356.2023.04.010
Cancer Biology

Screening ferroptosis related genes influencing prognosis of colon cancer through bioinformatics analysis

  • LI  Xiao-jun1  ZHANG Ya-min2*
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Abstract

Objective  To explore ferroptosis-related long non-coding RNAs (lncRNAs) with prognostic significance in colon cancer (CC), and then construct a prognosis-related predictive scoring model. To search for ferroptosis-related differential expressed genes co-expressed with prognosis-related lncRNAs.    Methods  Ferroptosis-related genes (FGs) were downloaded from FerrDb database; The expression data of 41 adjacent normal tissues and 473 tumor tissues, and clinical data of 452 patients were successfully downloaded. Co-expression and differential expression analysis was performed to identify differentially expressed ferroptosis-related lncRNAs (DEFlncRNAs), and univariate Cox regression analysis was used to screen statistically significant prognosis-related DEFlncRNAs, and then multivariate Cox regression analysis was used to construct a prognostic model, calculate risk score among CC patients and divide patients by the median risk score. Kaplan-Meier curves, univariate and multivariate Cox regression analyses, and receiver operationg characteristic(ROC) curve were used to reveale great accuracy of the model. Then, a nomogram was drawed to predict the survival among CC patients. Finally, the differentially expressed ferroptosis-related genes regulating DEFlncRNAs were found by co-expression analysis, and the different expression was verified by immunohistochemical experiments.    Result  Expression and clinical data among colon cancer (CC) patients were downloaded from TCGA database. A risk prognostic model containing 28 lncRNAs to predict the prognosis among CC patients was successfully constructed. An effective clinical nomogram for predicting the overall survival of CC patients was successfully constructed. Finally, the co-expression analysis of DEFlncRNAs and differentially expressed ferroptosis-related genes (DEFGs) was preformed to obtain a co-expression network, including17 key DEFGs, with the correlation coefficient filter criteria (|corFilter|)>0.4 and  P value filter criteria (P value filter)<0.05. Immunohistochemical experiments confirmed ANGPTL7 was highly expressed in the adjacent tissues among CC patients.    Conclusion  Successfully constructed a prognostic-related model among CC patients containing 28 DEFlncRNAs, and 17 DEFGs was finally obtained. 

Key words

Ferroptosis / Coloncellular carcinoma / Prognostic model / Bioinformatics / Cox regression analysis / Human

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LI Xiao-jun ZHANG Ya-min. Screening ferroptosis related genes influencing prognosis of colon cancer through bioinformatics analysis[J]. Acta Anatomica Sinica. 2023, 54(4): 445-452 https://doi.org/10.16098/j.issn.0529-1356.2023.04.010

References

[1]Dixon SJ, Lemberg KM, Lamprecht MR, et al. Ferroptosis: an iron-dependent form of nonapoptotic cell death[J]. Cell, 2012, 149(5): 1060-1072. 
[2]Hassannia B, Vandenabeele P, Vanden BT. Targeting ferroptosis to iron out cancer[J]. Cancer Cell, 2019, 35(6): 830-849. 
[3]Guo J, Xu B, Han Q, et al. Ferroptosis: a novel anti-tumor action for cisplatin[J]. Cancer Res Treat, 2018, 50(2): 445-460. 
[4]Park S, Oh J, Kim M, et al. Bromelain effectively suppresses Kras-mutant colorectal cancer by stimulating ferroptosis[J]. Anim Cells Syst(Seoul), 2018, 22(5): 334-340. 
[5]Gotwals P, Cameron S, Cipolletta D, et al. Prospects for combining targeted and conventional cancer therapy with immunotherapy[J]. Nat Rev Cancer, 2017, 17(5): 286-301. 
[6]Li HD, Yang Ch. Wiskot -Aldrich syndrome-like lower expressed in colon cancer tissues and inhibited the stemness of human colon cancer[J]. Acta Anatomica Sinica, 2022, 53(1): 50-59.(in Chinese)
李宏丹,杨成. WAS-like 蛋白在肠癌组织中低表达并抑制人结肠癌细胞的干性[J]. 解剖学报, 2022, 53(1): 50-59.
 [7]Wu G, Yuan S, Chen Z, et al. The KLF14 transcription factor regulates glycolysis by downregulating LDHB in colorectal cancer[J]. Int J Biol Sci, 2019, 15(3): 628-635. 
[8]Cohen JH, Kristal AR, Stanford JL. Fruit and vegetable intakes and prostate cancer risk[J].  J Natl Cancer Inst, 2000, 92(1): 61-68. 
[9]Bianchini F, Kaaks R, Vainio H. Overweight, obesity, and cancer risk[J]. Lancet Oncol, 2002, 3(9): 565-574. 
[10]Shen Z, Song J, Yung BC, et al. Emerging strategies of cancer therapy based on ferroptosis[J]. Adv Mater, 2018, 30(12): e1704007. 
[11]Liu ShH, Wang W, Mu XS. Expression of Golgi phosphoprotein 3 in colorectal cancer tissues and its effects on proliferation,invasion and migration of colorectal cancer cells [J]. Acta Anatomica Sinica, 2018,49(4):461-468. (in Chinese)
刘师宏,汪威,穆小松. 高尔基体磷蛋白3在结直肠癌组织中表达及其对结直肠癌细胞增殖、侵袭和迁移的影响[J]. 解剖学报, 2018, 49(4): 461-468.
[12]Liu X, Zhang Y, Wu S, et al. Palmatine induces G2/M phase arrest and mitochondrial-associated pathway apoptosis in colon cancer cells by targeting AURKA[J]. Biochem Pharmacol, 2020, 175: 113933. 
[13]Wang-Bishop L, Chen Z, Gomaa A, et al. Inhibition of AURKA reduces proliferation and survival of gastrointestinal cancer cells with activated KRAS by preventing activation of RPS6KB1[J]. Gastroenterology, 2019, 156(3): 662-675. 
[14]Li T, Chen Y, Zhang J, et al. LncRNA TUG1 promotes cells proliferation and inhibits cells apoptosis through regulating AURKA in epithelial ovarian cancer cells[J]. Medicine, 2018, 97(36): e12131. 
[15]Deb M, Sengupta D, Kar S, et al. Epigenetic drift towards histone modifications regulates CAV1 gene expression in colon cancer[J]. Gene, 2016, 581(1): 75-84. 
[16]Luo Z, Rong Z, Zhang J, et al. Circular RNA circCCDC9 acts as a miR-6792-3p sponge to suppress the progression of gastric cancer through regulating CAV1 expression[J]. Mol Cancer, 2020, 19(1): 86. 
[17]Campos A, Salomon C, Bustos R, et al. Caveolin-1-containing extracellular vesicles transport adhesion proteins and promote malignancy in breast cancer cell lines[J]. Nanomedicine (Lond), 2018, 13(20): 2597-2609. 
[18]Wang X, Tao G, Huang D, et al. Circular RNA NOX4 promotes the development of colorectal cancer via the microRNA-485-5p/CKS1B axis[J]. Oncol Rep, 2020, 44(5): 2009-2020. 
[19]Venè R, Costa D, Augugliaro R, et al. Evaluation of glycosylated PTGS2 in colorectal cancer for NSAIDS-Based adjuvant therapy[J]. Cells, 2020, 9(3): 683. [20]Yang Y, Lin J, Guo S, et al. RRM2 protects against ferroptosis and is a tumor biomarker for liver cancer[J]. Cancer Cell Int, 2020, 20(1): 587. 
[21]Zhang Z, Du J, Wang S, et al. OTUB2 Promotes cancer metastasis via hippo-independent activation of YAP and TAZ[J]. Mol Cell, 2019, 73(1): 7-21. 
[22]Yao X, He Z, Qin C, et al. SLC2A3 promotes macrophage infiltration by glycolysis reprogramming in gastric cancer[J]. Cancer Cell Int, 2020, 20: 503. 
[23]Cuzziol CI, Castanhole-Nunes M, Pavarino éC, et al. MicroRNAs as regulators of VEGFA and NFE2L2 in cancer[J]. Gene, 2020, 759: 144994. 
[24]Krebs AM, Mitschke J, Lasierra Losada M, et al. The EMT-activator Zeb1 is a key factor for cell plasticity and promotes metastasis in pancreatic cancer
[J] . Nat Cell Biol, 2017, 19(5): 518-529. 
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