血清趋化因子配体20、叉头框D1对宫颈癌患者放化疗后复发、转移的预测价值

郜蕾, 袁香坤, 胡建伟, 张永侠, 苗珺珺, 田丹丹, 侯光营, 陈媛媛, 王晴雯, 王玺

肿瘤代谢与营养电子杂志 ›› 2026, Vol. 13 ›› Issue (3) : 421-427.

PDF(1705 KB)
PDF(1705 KB)
肿瘤代谢与营养电子杂志 ›› 2026, Vol. 13 ›› Issue (3) : 421-427. DOI: 10.16689/j.cnki.cn11-9349/r.2026.03.014
论著

血清趋化因子配体20、叉头框D1对宫颈癌患者放化疗后复发、转移的预测价值

  • 郜蕾, 袁香坤, 胡建伟, 张永侠, 苗珺珺, 田丹丹, 侯光营, 陈媛媛, 王晴雯, 王玺
作者信息 +

The predictive value of serum CCL20 and FOXD1 for relapse and metastasis in cervical cancer patients after radiotherapy and chemotherapy

  • Gao Lei, Yuan Xiangkun, Hu Jianwei, Zhang Yongxia, Miao Junjun, Tian Dandan, Hou Guangying, Chen Yuanyuan, Wang Qingwen, Wang Xi
Author information +
文章历史 +

摘要

目的 探讨血清趋化因子配体20(CCL20)、叉头框D1(FOXD1)对宫颈癌患者放化疗后复发、转移的预测价值。方法 选取河北省沧州中西医结合医院2021年3月至2024年2月进行放化疗后的宫颈癌患者134例作为研究组,根据患者是否复发、转移将其分为复发组(n=38)、未复发组(n=96),选取同期130例宫颈良性病变患者(病变组)和100例健康体检者(对照组)进行比较。采用ELISA法检测血清CCL20、FOXD1表达水平,并比较复发组与未复发组临床病理特征及血清CCL20、FOXD1表达水平;采用多因素Logistic回归分析放化疗后宫颈癌患者复发、转移的影响因素,受试者操作特征(ROC)曲线评估血清CCL20、FOXD1的预测价值;决策曲线分析(DCA)预测模型的临床价值。结果 血清CCL20和FOXD1水平呈梯度升高(研究组>病变组>对照组,P<0.05)。复发组肿瘤分期Ⅳ期、有淋巴结转移、浸润深度≥1/2占比及血清CCL20、FOXD1水平均高于未复发组(P<0.05)。这些因素均是放化疗后宫颈癌患者复发、转移的独立危险因素(P<0.05)。血清CCL20、FOXD1及联合预测宫颈癌患者放化疗后复发、转移的曲线下面积(AUC)分别为0.844、0.859及0.936,优于各自单独预测(Z联合-CCL20=2.887、Z联合-FOXD1=2.241,P=0.004、P=0.025)。DCA结果显示,当阈值概率范围为0.04~0.98时,血清CCL20、FOXD1联合预测宫颈癌患者放化疗后复发、转移的净获益率高于单一指标预测。结论 宫颈癌患者血清CCL20、FOXD1表达水平均明显升高,二者联合检测对宫颈癌患者放化疗后复发、转移可能有更高的临床预测价值。

Abstract

Objective To explore the predictive value of serum chemokine ligand 20 (CCL20) and forkhead box D1 (FOXD1) for relapse and metastasis in cervical cancer patients after radiotherapy and chemotherapy. Method From March 2021 to February 2024, 134 patients with cervical cancer who underwent radiotherapy and chemotherapy in Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine, Hebei Province were designated as the study group. They were grouped into a relapse group (n=38) and a non-relapsing group (n=96) based on whether they had relapse or metastasis. Meanwhile, 130 patients with benign cervical lesions were served as the lesion group. Another 100 healthy individuals who underwent physical examination were served as the control group. ELISA method was used to detect serum CCL20 and FOXD1. The clinical pathological features, as well as serum CCL20 and FOXD1, were compared between the relapse and non-relapsing groups. Multivariate logistic regression was used to explore the influencing factors of relapse and metastasis in cervical cancer patients after radiotherapy and chemotherapy. ROC curve was used to explore the predictive value of serum CCL20 and FOXD1 for relapse and metastasis in cervical cancer patients after radiotherapy and chemotherapy. Decision curve (DCA) analysis for predicting the clinical value of the model. Result Serum CCL20 and FOXD1 levels showed a gradient increase (study group> lesion group> control group, P<0.05). The relapse group had higher proportions of tumor stage Ⅳ, lymph node metastasis, infiltration depth ≥1/2, and levels of serum CCL20 and FOXD1 than the non-relapse group (P<0.05). All these factors were independent risk factors for recurrence and metastasis after chemoradiotherapy (P<0.05). The area under the curve (AUC) values of serum CCL20, FOXD1, and their combination in predicting relapse and metastasis in cervical cancer patients after radiotherapy and chemotherapy were 0.844, 0.859, and 0.936, respectively. The combination was better than the individual predictions (Z combination - CCL20=2.887, Z combination - FOXD1=2.241, P=0.004, P=0.025). The results of DCA curve analysis showed that when the high-risk threshold was 0.04 to 0.98, the net benefit rate of the combined prediction of serum CCL20 and FOXD1 for recurrence and metastasis of cervical cancer patients after radiotherapy and chemotherapy was higher than that predicted by a single indicator. Conclusion The expression levels of CCL20 and FOXD1 in the serum of cervical cancer patients were significantly elevated, and the combined detection may have higher predictive value for recurrence and metastasis after chemoradiotherapy in cervical cancer patients.

关键词

宫颈癌 / 趋化因子配体20 / 叉头框D1 / 放化疗 / 复发 / 转移 / 预测价值 / 预后

Key words

Cervical cancer / Chemokine ligand 20 / Forkhead box D1 / Radiotherapy and chemotherapy / Relapse / Metastasis / Measurement value / Prognosis

引用本文

导出引用
郜蕾, 袁香坤, 胡建伟, 张永侠, 苗珺珺, 田丹丹, 侯光营, 陈媛媛, 王晴雯, 王玺. 血清趋化因子配体20、叉头框D1对宫颈癌患者放化疗后复发、转移的预测价值[J]. 肿瘤代谢与营养电子杂志. 2026, 13(3): 421-427 https://doi.org/10.16689/j.cnki.cn11-9349/r.2026.03.014
Gao Lei, Yuan Xiangkun, Hu Jianwei, Zhang Yongxia, Miao Junjun, Tian Dandan, Hou Guangying, Chen Yuanyuan, Wang Qingwen, Wang Xi. The predictive value of serum CCL20 and FOXD1 for relapse and metastasis in cervical cancer patients after radiotherapy and chemotherapy[J]. Electronic Journal of Metabolism and Nutrition of Cancer. 2026, 13(3): 421-427 https://doi.org/10.16689/j.cnki.cn11-9349/r.2026.03.014

参考文献

[1] SAHASRABUDDHE V V. Cervical cancer: precursors and prevention[J]. Hematol Oncol Clin North Am, 2024, 38(4):771-781.
[2] MANRRIQUEZ E N, ZAKHOUR M, SALANI R. Precision medicine for cervical cancer[J]. Curr Opin Obstet Gynecol, 2022, 34(1):1-5.
[3] 张羽, 张凯悦, 贾好东,等. 基于IVIM-DWI及影像组学的列线图预测宫颈癌同步放化疗后复发[J]. 中华放射肿瘤学杂志, 2022, 31(10):897-903.
[4] MAYADEV J S, KE G, MAHANTSHETTY U, et al. Global challenges of radiotherapy for the treatment of locally advanced cervical cancer[J]. Int J Gynecol Cancer, 2022, 32(3):436-445.
[5] AKINYEMI O, OGUNYANKIN F, FASOKUN M, et al. Medicaid expansion and overall mortality among women with cervical cancer[J]. Int J Gynaecol Obstet, 2026, 172(1):343-350.
[6] LIN Z, LI X, SHI H, et al. Decoding the tumor microenvironment and molecular mechanism: unraveling cervical cancer subpopulations and prognostic signatures through scRNA-Seq and bulk RNA-seq analyses[J]. Front Immunol, 2024, 15(1):1351287.
[7] KWANTWI L B, BOAFO J D, EGLEH B E, et al. CCL20 in the tumor microenvironment: implications for cancer progression and therapeutic approaches[J]. Clin Transl Oncol, 2025, 27(8):3285-3292.
[8] JIA H M, ARIFU A, WANG J J, et al. SPP1 enhances radiotherapy resistance through CCL2-mediated M2-like polarization of macrophages in cervical cancer[J]. Int Immunopharmacol, 2026, 172:116119.
[9] CHEN S, YANG M, WANG C, et al. Forkhead box D1 promotes EMT and chemoresistance by upregulating lncRNA CYTOR in oral squamous cell carcinoma[J]. Cancer Lett, 2021, 503(1):43-53.
[10] BHATLA N, DENNY L. FIGO cancer report 2018[J]. Int J Gynaecol Obstet, 2018, 143(2):2-3.
[11] JHA A K, MITHUN S, SHERKHANE U B, et al. Systematic review and meta-analysis of prediction models used in cervical cancer[J]. Artif Intell Med, 2023, 139(1):102549.
[12] CARUSO G, WAGAR M K, HSU H C, et al. Cervical cancer: a new era[J]. Int J Gynecol Cancer, 2024, 34(12):1946-1970.
[13] GOPU P, ANTONY F, CYRIAC S, et al. Updates on systemic therapy for cervical cancer[J]. Indian J Med Res, 2021, 154(2):293-302.
[14] REVATHIDEVI S, MURUGAN A K, NAKAOKA H, et al. APOBEC: a molecular driver in cervical cancer pathogenesis[J]. Cancer Lett, 2021, 496(1):104-116.
[15] WŁOSZEK E, KRUPA K, SKROK E, et al. HPV and cervical cancer-biology, prevention, and treatment updates[J]. Curr Oncol, 2025, 32(3):122.
[16] RAJARAM S, GUPTA B. Screening for cervical cancer: choices & dilemmas[J]. Indian J Med Res, 2021, 154(2):210-220.
[17] LI Y, GENG W L, LI C C, et al. Progress of CCL20-CCR6 in the airways: a promising new therapeutic target[J]. J Inflamm (Lond), 2024, 21(1):54.
[18] STALLHOFER J, REICHL F, LAUSEKER M, et al. CCL20 expression is elevated in inflammatory bowel disease and attenuated by vitamin D metabolites[J]. Sci Rep, 2025, 15(1):20145.
[19] KWANTWI L B, WANG S, SHENG Y, et al. Multifaceted roles of CCL20 (C-C motif chemokine ligand 20): mechanisms and communication networks in breast cancer progression[J]. Bioengineered, 2021, 12(1):6923-6934.
[20] ZHANG R, DONG M, TU J, et al. PMN-MDSCs modulated by CCL20 from cancer cells promoted breast cancer cell stemness through CXCL2-CXCR2 pathway[J]. Signal Transduct Target Ther, 2023, 8(1):97.
[21] XU C, FAN L, LIN Y, et al. Fusobacterium nucleatum promotes colorectal cancer metastasis through miR-1322/CCL20 axis and M2 polarization[J]. Gut Microbes, 2021, 13(1):1980347.
[22] YU Y, LIU Y, LI Y, et al. Construction of a CCL20-centered circadian-signature based prognostic model in cervical cancer[J]. Cancer Cell Int, 2023, 23(1):92.
[23] 王瑾琳, 张颖杰, 郭锐. 血清CCL20、β2-MG与乳腺癌患者术后复发转移及预后的关系[J]. 实用癌症杂志, 2024, 39(4):667-670.
[24] FERNANDES A T G, CARVALHO M O O, AVVAD-PORTARI E, et al. A prognostic value of CD45RA+, CD45RO+, CCL20+ and CCR6+ expressing cells as 'immunoscore' to predict cervical cancer induced by HPV[J]. Sci Rep, 2021, 11(1):8782.
[25] HUANG J, LIANG B, WANG T. FOXD1 expression in head and neck squamous carcinoma: a study based on TCGA, GEO and meta-analysis[J]. Biosci Rep, 2021, 41(7):BSR20210158.
[26] BOND K H, SIMS-LUCAS S, OXBURGH L. Targets for renal carcinoma growth control identified by screening FOXD1 cell proliferation pathways[J]. Cancers (Basel), 2022, 14(16):3958.
[27] ANJUM H, SMITH J P, MARTINI A G, et al. Tcf21 as a founder transcription factor in specifying Foxd1 cells to the juxtaglomerular cell lineage[J]. Am J Physiol Renal Physiol, 2025, 328(1):F121-F130.
[28] HUANG Y, ZHANG L, LIU T, et al. LMNB1 targets FOXD1 to promote progression of prostate cancer[J]. Exp Ther Med, 2023, 26(5):513.
[29] CAI K, CHEN S, ZHU C, et al. FOXD1 facilitates pancreatic cancer cell proliferation, invasion, and metastasis by regulating GLUT1-mediated aerobic glycolysis[J]. Cell Death Dis, 2022, 13(9):765.
[30] 明霞, 刘伟. 血清叉头框D1在鼻咽癌患者中的表达及其与放疗后复发转移关系研究[J]. 陕西医学杂志, 2024, 53(11):1495-1499.
[31] WU T, YANG Z, CHEN W, et al. MiR-30e-5p-mediated FOXD1 promotes cell proliferation by blocking cellular senescence and apoptosis through p21/CDK2/Rb signaling in head and neck carcinoma[J]. Cell Death Discov, 2023, 9(1):295.
[32] LI J, YAN T, WU X, et al. Aberrant overexpression of transcription factor Forkhead box D1 predicts poor prognosis and promotes cancer progression in HNSCC[J]. BMC Cancer, 2021, 21(1):1205.
[33] GAO J, WU S. FOXD1, a hypoxia-related gene, accelerates prostate cancer cell growth by increasing glycolysis under hypoxia conditions[J]. BMC Biotechnol, 2025, 25(1):123.
[34] LONG Y, CHONG T, LYU X, et al. FOXD1-dependent RalA-ANXA2-Src complex promotes CTC formation in breast cancer[J]. J Exp Clin Cancer Res, 2022, 41(1):301.
[35] WEN K, WANG L, SU H, et al. Development of a m6A- and ferroptosis-related LncRNA signature for forecasting prognosis and treatment response in cervical cancer[J]. BMC Cancer, 2025, 25(1):580.

PDF(1705 KB)

Accesses

Citation

Detail

段落导航
相关文章

/