General Research Article

调节性T细胞,妊娠,COVID-19,感染,Tregs, SARS冠状病毒。

卷 31, 期 26, 2024

发表于: 14 February, 2024

页: [4213 - 4231] 页: 19

弟呕挨: 10.2174/0109298673281438231217151129

open access plus

摘要

背景:卵巢癌(OC)是女性中最致命的恶性肿瘤,由于耐药和缺乏对抗癌药物治疗反应的预测工具,预后较差。目的:本研究的目的是建立一个预测OC患者治疗反应的模型。 方法:RNA-seq技术用于鉴定差异表达的紫杉醇(PTX)耐药lncRNAs (DE-lncRNAs)。使用Cancer Genome Atlas (TCGA)-OV和import数据库获取免疫相关lncRNAs (ir-lncRNAs)。采用单因素、多因素和LASSO Cox回归分析构建预测模型。Kaplan- meier绘图图、主成分分析(PCA)、nomogram、免疫功能分析和治疗反应应用于癌症药物敏感性基因组学(GDSC)、CIBERSORT和TCGA数据库。在CCLE数据库和OC细胞中评估其生物学功能。 结果:RNA-seq确定了ptx耐药A2780- ptx和ptx敏感A2780细胞之间的186个de - lncrna。通过对TCGA-OV数据库的分析,鉴定出225个ir- lncrna。通过单因素、多因素和LASSO Cox回归分析,对186个de - lncrna和225个ir- lncrna进行分析,发现9个ptx耐药免疫相关lncrna (deir - lncrna)作为生物标志物,可作为预测模型中的潜在生物标志物。OC的单细胞RNA测序(scRNA-seq)数据证实了DEir-lncRNAs与免疫反应性的相关性。预测评分低的患者预后良好,而预测评分高的患者更容易逃避免疫治疗和化疗,预后较差。 结论:由9个deir - lncrna组成的新预测模型是预测OC患者免疫治疗和化疗反应和预后的有价值的工具。

关键词: 生物标志物,化疗耐药,DEir-lncRNAs,免疫治疗,非编码RNA,预测工具,scRNA- seq。

« Previous
[1]
Kuroki, L.; Guntupalli, S.R. Treatment of epithelial ovarian cancer. BMJ, 2020, 371, m3773.
[http://dx.doi.org/10.1136/bmj.m3773] [PMID: 33168565]
[2]
Siegel, R.L.; Miller, K.D.; Wagle, N.S.; Jemal, A. Cancer statistics, 2023. CA Cancer J. Clin., 2023, 73(1), 17-48.
[http://dx.doi.org/10.3322/caac.21763] [PMID: 36633525]
[3]
Thusgaard, C.F.; Korsholm, M.; Koldby, K.M.; Kruse, T.A.; Thomassen, M.; Jochumsen, K.M. Epithelial ovarian cancer and the use of circulating tumor DNA: A systematic review. Gynecol. Oncol., 2021, 161(3), 884-895.
[http://dx.doi.org/10.1016/j.ygyno.2021.04.020] [PMID: 33892886]
[4]
Das, T; Anand, U; Pandey, SK; Ashby, CR, Jr; Assaraf, YG; Chen, ZS Therapeutic strategies to overcome taxane resistance in cancer. Drug resistance updates: Reviews and commentaries in antimicrobial and anticancer chemotherapy. 2021, 55, 100754.
[http://dx.doi.org/10.1016/j.drup.2021.100754]
[5]
Tymon-Rosario, J.; Adjei, N.N.; Roque, D.M.; Santin, A.D. Microtubule-interfering drugs: Current and future roles in epithelial ovarian cancer treatment. Cancers, 2021, 13(24), 6239.
[http://dx.doi.org/10.3390/cancers13246239] [PMID: 34944858]
[6]
Baird, R.D.; Tan, D.S.P.; Kaye, S.B. Weekly paclitaxel in the treatment of recurrent ovarian cancer. Nat. Rev. Clin. Oncol., 2010, 7(10), 575-582.
[http://dx.doi.org/10.1038/nrclinonc.2010.120] [PMID: 20683437]
[7]
Markman, M.; Mekhail, T.M. Paclitaxel in cancer therapy. Expert Opin. Pharmacother., 2002, 3(6), 755-766.
[http://dx.doi.org/10.1517/14656566.3.6.755] [PMID: 12036415]
[8]
Sharma, S.; Salomon, C. Techniques associated with exosome isolation for biomarker development: Liquid biopsies for ovarian cancer detection. Methods Mol. Biol., 2020, 2055, 181-199.
[http://dx.doi.org/10.1007/978-1-4939-9773-2_8] [PMID: 31502152]
[9]
Newick, K.; O’Brien, S.; Moon, E.; Albelda, S.M. CAR T cell therapy for solid tumors. Annu. Rev. Med., 2017, 68(1), 139-152.
[http://dx.doi.org/10.1146/annurev-med-062315-120245] [PMID: 27860544]
[10]
Lan, H.; Yuan, J.; Zeng, D.; Liu, C.; Guo, X.; Yong, J.; Zeng, X.; Xiao, S. The emerging role of non-coding RNAs in drug resistance of ovarian cancer. Front. Genet., 2021, 12, 693259.
[http://dx.doi.org/10.3389/fgene.2021.693259] [PMID: 34512721]
[11]
Braga, E.A.; Fridman, M.V.; Moscovtsev, A.A.; Filippova, E.A.; Dmitriev, A.A.; Kushlinskii, N.E. LncRNAs in ovarian cancer progression, metastasis, and main pathways: ceRNA and alternative mechanisms. Int. J. Mol. Sci., 2020, 21(22), 8855.
[http://dx.doi.org/10.3390/ijms21228855] [PMID: 33238475]
[12]
Song, Y.; Qu, H. Identification and validation of a seven m6A-related lncRNAs signature predicting prognosis of ovarian cancer. BMC Cancer, 2022, 22(1), 633.
[http://dx.doi.org/10.1186/s12885-022-09591-4] [PMID: 35676619]
[13]
Zheng, J.; Guo, J.; Wang, Y.; Zheng, Y.; Zhang, K.; Tong, J. Bioinformatic analyses of the ferroptosis-related lncrnas signature for ovarian cancer. Front. Mol. Biosci., 2022, 8, 735871.
[http://dx.doi.org/10.3389/fmolb.2021.735871] [PMID: 35127813]
[14]
Zheng, J.; Guo, J.; Zhu, L.; Zhou, Y.; Tong, J. Comprehensive analyses of glycolysis-related lncRNAs for ovarian cancer patients. J. Ovarian Res., 2021, 14(1), 124.
[http://dx.doi.org/10.1186/s13048-021-00881-2] [PMID: 34560889]
[15]
Zhang, Z.; Xu, Z.; Yan, Y. Role of a pyroptosis-related lncRNA signature in risk stratification and immunotherapy of ovarian cancer. Front. Med., 2022, 8, 793515.
[http://dx.doi.org/10.3389/fmed.2021.793515] [PMID: 35096881]
[16]
Li, H.; Liu, Z.Y.; Chen, Y.C.; Zhang, X.Y.; Wu, N.; Wang, J. Identification and validation of an immune-related lncRNAs signature to predict the overall survival of ovarian cancer. Front. Oncol., 2022, 12, 999654.
[http://dx.doi.org/10.3389/fonc.2022.999654] [PMID: 36313727]
[17]
Lheureux, S.; Gourley, C.; Vergote, I.; Oza, A.M. Epithelial ovarian cancer. Lancet, 2019, 393(10177), 1240-1253.
[http://dx.doi.org/10.1016/S0140-6736(18)32552-2] [PMID: 30910306]
[18]
Torre, L.A.; Trabert, B.; DeSantis, C.E.; Miller, K.D.; Samimi, G.; Runowicz, C.D.; Gaudet, M.M.; Jemal, A.; Siegel, R.L. Ovarian cancer statistics, 2018. CA Cancer J. Clin., 2018, 68(4), 284-296.
[http://dx.doi.org/10.3322/caac.21456] [PMID: 29809280]
[19]
Rodolakis, I.; Pergialiotis, V.; Liontos, M.; Haidopoulos, D.; Loutradis, D.; Rodolakis, A.; Bamias, A.; Thomakos, N. Chemotherapy response score in ovarian cancer patients: An overview of its clinical utility. J. Clin. Med., 2023, 12(6), 2155.
[http://dx.doi.org/10.3390/jcm12062155] [PMID: 36983157]
[20]
Atallah, G.A.; Kampan, N.C.; Chew, K.T.; Mohd Mokhtar, N.; Md Zin, R.R.; Shafiee, M.N.B.; Abd Aziz, N.H.B. Predicting prognosis and platinum resistance in ovarian cancer: Role of immunohistochemistry biomarkers. Int. J. Mol. Sci., 2023, 24(3), 1973.
[http://dx.doi.org/10.3390/ijms24031973] [PMID: 36768291]
[21]
Jin, Y.; Cao, J.; Cheng, H.; Hu, X. LncRNA POU6F2-AS2 contributes to malignant phenotypes and paclitaxel resistance by promoting SKP2 expression in stomach adenocarcinoma. J. Chemother., 2023, 35(7), 638-652.
[http://dx.doi.org/10.1080/1120009X.2023.2177807] [PMID: 36797828]
[22]
Zhao, H.; Wang, A.; Zhang, Z. LncRNA SDHAP1 confers paclitaxel resistance of ovarian cancer by regulating EIF4G2 expression via miR-4465. J. Biochem., 2020, 168(2), 171-181.
[http://dx.doi.org/10.1093/jb/mvaa036] [PMID: 32211849]
[23]
Chen, W.; Yan, L.; Long, B.; Lin, L. Identification of immune-related lncRNAs for predicting prognosis and immune landscape characteristics of uveal melanoma. J. Oncol., 2022, 2022, 1-12.
[http://dx.doi.org/10.1155/2022/7680657] [PMID: 36405245]
[24]
Xing, X.L.; Xing, C.; Huang, Z.; Yao, Z.Y.; Liu, Y.W. Immune-related lncRNAs to construct novel signatures and predict the prognosis of rectal cancer. Front. Oncol., 2021, 11, 661846.
[http://dx.doi.org/10.3389/fonc.2021.661846] [PMID: 34485113]
[25]
Cioffi, R.; Bergamini, A.; Rabaiotti, E.; Petrone, M.; Pella, F.; Ferrari, D.; Mangili, G.; Candiani, M. Neoadjuvant chemotherapy in high-risk ovarian cancer patients: Role of age. Tumori, 2019, 105(2), 168-173.
[http://dx.doi.org/10.1177/0300891618792468] [PMID: 30157707]
[26]
Tajik, P.; van de Vrie, R.; Zafarmand, M.H.; Coens, C.; Buist, M.R.; Vergote, I. The FIGO stage IVA versus IVB of ovarian cancer: Prognostic value and predictive value for neoadjuvant chemotherapy. International journal of gynecological cancer. 2018, 28(3), 453-458.
[http://dx.doi.org/10.1097/IGC.0000000000001186]
[27]
Nasioudis, D.; Ko, E.M.; Haggerty, A.F.; Giuntoli, R.L., II; Burger, R.A.; Morgan, M.A.; Latif, N.A. Isolated distant lymph node metastases in ovarian cancer. Should a new substage be created? Gynecol. Oncol. Rep., 2019, 28, 86-90.
[http://dx.doi.org/10.1016/j.gore.2019.03.008] [PMID: 30976643]
[28]
Liang, W.; Wang, L.; Li, H.; Liu, C.; Wu, M.; Li, J. The added value of CA125 normalization before interval debulking surgery to the chemotherapy response score for the prognostication of ovarian cancer patients receiving neoadjuvant chemotherapy for advanced disease. J. Cancer, 2021, 12(3), 946-953.
[http://dx.doi.org/10.7150/jca.52711] [PMID: 33403051]
[29]
Klotz, D.M.; Link, T.; Wimberger, P.; Kuhlmann, J.D. A predictive and prognostic model for surgical outcome and prognosis in ovarian cancer computed by clinico-pathological and serological parameters (CA125, HE4, mesothelin). Clin. Chem. Lab. Med., 2023.
[http://dx.doi.org/10.1515/cclm-2023-0314]
[30]
Métairie, M.; Benoit, L.; Koual, M.; Bentivegna, E.; Wohrer, H.; Bolze, P.A.; Kerbage, Y.; Raimond, E.; Akladios, C.; Carcopino, X.; Canlorbe, G.; Uzan, J.; Lavoué, V.; Mimoun, C.; Huchon, C.; Koskas, M.; Costaz, H.; Margueritte, F.; Dabi, Y.; Touboul, C.; Bendifallah, S.; Ouldamer, L.; Delanoy, N.; Nguyen-Xuan, H.T.; Bats, A.S.; Azaïs, H. A suggested modification to FIGO stage IV epithelial ovarian cancer. Cancers, 2023, 15(3), 706.
[http://dx.doi.org/10.3390/cancers15030706] [PMID: 36765667]
[31]
Zhu, J.W.; Wong, F.; Szymiczek, A.; Ene, G.E.V.; Zhang, S.; May, T.; Narod, S.A.; Kotsopoulos, J.; Akbari, M.R. Evaluating the utility of ctDNA in detecting residual cancer and predicting recurrence in patients with serous ovarian cancer. Int. J. Mol. Sci., 2023, 24(18), 14388.
[http://dx.doi.org/10.3390/ijms241814388] [PMID: 37762691]
[32]
Lu, H.; Arshad, M.; Thornton, A.; Avesani, G.; Cunnea, P.; Curry, E.; Kanavati, F.; Liang, J.; Nixon, K.; Williams, S.T.; Hassan, M.A.; Bowtell, D.D.L.; Gabra, H.; Fotopoulou, C.; Rockall, A.; Aboagye, E.O. A mathematical-descriptor of tumor-mesoscopic-structure from computed-tomography images annotates prognostic- and molecular-phenotypes of epithelial ovarian cancer. Nat. Commun., 2019, 10(1), 764.
[http://dx.doi.org/10.1038/s41467-019-08718-9] [PMID: 30770825]
[33]
Weigelt, B.; Vargas, H.A.; Selenica, P.; Geyer, F.C.; Mazaheri, Y.; Blecua, P.; Conlon, N.; Hoang, L.N.; Jungbluth, A.A.; Snyder, A.; Ng, C.K.Y.; Papanastasiou, A.D.; Sosa, R.E.; Soslow, R.A.; Chi, D.S.; Gardner, G.J.; Shen, R.; Reis-Filho, J.S.; Sala, E. Radiogenomics analysis of intratumor heterogeneity in a patient with high-grade serous ovarian cancer. JCO Precis. Oncol., 2019, 3(3), 1-9.
[http://dx.doi.org/10.1200/PO.18.00410] [PMID: 32914032]
[34]
Crispin-Ortuzar, M.; Woitek, R.; Reinius, M.A.V.; Moore, E.; Beer, L.; Bura, V.; Rundo, L.; McCague, C.; Ursprung, S.; Escudero Sanchez, L.; Martin-Gonzalez, P.; Mouliere, F.; Chandrananda, D.; Morris, J.; Goranova, T.; Piskorz, A.M.; Singh, N.; Sahdev, A.; Pintican, R.; Zerunian, M.; Rosenfeld, N.; Addley, H.; Jimenez-Linan, M.; Markowetz, F.; Sala, E.; Brenton, J.D. Integrated radiogenomics models predict response to neoadjuvant chemotherapy in high grade serous ovarian cancer. Nat. Commun., 2023, 14(1), 6756.
[http://dx.doi.org/10.1038/s41467-023-41820-7] [PMID: 37875466]
[35]
Sharbatoghli, M.; Vafaei, S.; Aboulkheyr Es, H.; Asadi-Lari, M.; Totonchi, M.; Madjd, Z. Prediction of the treatment response in ovarian cancer: A ctDNA approach. J. Ovarian Res., 2020, 13(1), 124.
[http://dx.doi.org/10.1186/s13048-020-00729-1] [PMID: 33076944]
[36]
Dai, D.; Li, Q.; Zhou, P.; Huang, J.; Zhuang, H.; Wu, H.; Chen, B. Analysis of omics data reveals nucleotide excision repair-related genes signature in highly-grade serous ovarian cancer to predict prognosis. Front. Cell Dev. Biol., 2022, 10, 874588.
[http://dx.doi.org/10.3389/fcell.2022.874588] [PMID: 35769257]
[37]
Zhang, M.; Cheng, S.; Jin, Y.; Zhao, Y.; Wang, Y. Roles of CA125 in diagnosis, prediction, and oncogenesis of ovarian cancer. Biochim. Biophys. Acta Rev. Cancer, 2021, 1875(2), 188503.
[http://dx.doi.org/10.1016/j.bbcan.2021.188503] [PMID: 33421585]
[38]
Alegría-Baños, J.A.; Jiménez-López, J.C.; Vergara-Castañeda, A.; de León, D.F.C.; Mohar-Betancourt, A.; Pérez-Montiel, D.; Sánchez-Domínguez, G.; García-Villarejo, M.; Olivares-Pérez, C.; Hernández-Constantino, Á.; González-Santiago, A.; Clara-Altamirano, M.; Arela-Quispe, L.; Prada-Ortega, D. Kinetics of HE4 and CA125 as prognosis biomarkers during neoadjuvant chemotherapy in advanced epithelial ovarian cancer. J. Ovarian Res., 2021, 14(1), 96.
[http://dx.doi.org/10.1186/s13048-021-00845-6] [PMID: 34275472]
[39]
Zhang, M.; Wang, Y.; Xu, S.; Huang, S.; Wu, M.; Chen, G.; Wang, Y. Endoplasmic reticulum stress-related ten-biomarker risk classifier for survival evaluation in epithelial ovarian cancer and TRPM2: A potential therapeutic target of ovarian cancer. Int. J. Mol. Sci., 2023, 24(18), 14010.
[http://dx.doi.org/10.3390/ijms241814010] [PMID: 37762313]
[40]
Yang, J.; Wang, C.; Zhang, Y.; Cheng, S.; Xu, Y.; Wang, Y. A novel pyroptosis-related signature for predicting prognosis and evaluating tumor immune microenvironment in ovarian cancer. J. Ovarian Res., 2023, 16(1), 196.
[http://dx.doi.org/10.1186/s13048-023-01275-2] [PMID: 37730669]
[41]
Wang, X.; Wang, Y.; Sun, F.; Xu, Y.; Zhang, Z.; Yang, C.; Zhang, L.; Lou, G. Novel LncRNA ZFHX4-AS1 as a potential prognostic biomarker that affects the immune microenvironment in ovarian cancer. Front. Oncol., 2022, 12, 945518.
[http://dx.doi.org/10.3389/fonc.2022.945518] [PMID: 35903691]
[42]
Shi, X.; Guo, X.; Li, X.; Wang, M.; Qin, R. Loss of Linc01060 induces pancreatic cancer progression through vinculin-mediated focal adhesion turnover. Cancer Lett., 2018, 433, 76-85.
[http://dx.doi.org/10.1016/j.canlet.2018.06.015] [PMID: 29913236]
[43]
Li, J.; Liao, T.; Liu, H.; Yuan, H.; Ouyang, T.; Wang, J.; Chai, S.; Li, J.; Chen, J.; Li, X.; Zhao, H.; Xiong, N. Hypoxic glioma stem cell–derived exosomes containing linc01060 promote progression of glioma by regulating the MZF1/C-MYC/HIF1Α axis. Cancer Res., 2021, 81(1), 114-128.
[http://dx.doi.org/10.1158/0008-5472.CAN-20-2270] [PMID: 33158815]
[44]
Zhu, L.; Zhang, X.P.; Xu, S.; Hu, M.G.; Zhao, Z.M.; Zhao, G.D.; Xiao, Z.H.; Liu, R. Identification of a CD4+ conventional T cells-related lncRNAs signature associated with hepatocellular carcinoma prognosis, therapy, and tumor microenvironment. Front. Immunol., 2023, 13, 1111246.
[http://dx.doi.org/10.3389/fimmu.2022.1111246] [PMID: 36700197]
[45]
Li, L.; Han, J.; Zhang, S.; Dong, C.; Xiao, X. KIF26B-AS1 regulates TLR4 and activates the TLR4 signaling pathway to promote malignant progression of laryngeal cancer. J. Microbiol. Biotechnol., 2022, 32(10), 1344-1354.
[http://dx.doi.org/10.4014/jmb.2203.03037] [PMID: 36224753]
[46]
Yang, C.; Xia, B.R.; Zhang, Z.C.; Zhang, Y.J.; Lou, G.; Jin, W.L. Immunotherapy for ovarian cancer: Adjuvant, combination, and neoadjuvant. Front. Immunol., 2020, 11, 577869.
[http://dx.doi.org/10.3389/fimmu.2020.577869] [PMID: 33123161]
[47]
Margul, D.; Yu, C.; AlHilli, M.M. Tumor immune microenvironment in gynecologic cancers. Cancers, 2023, 15(15), 3849.
[http://dx.doi.org/10.3390/cancers15153849] [PMID: 37568665]
[48]
Colombo, I.; Karakasis, K.; Suku, S.; Oza, A.M. Chasing immune checkpoint inhibitors in ovarian cancer: Novel combinations and biomarker discovery. Cancers, 2023, 15(12), 3220.
[http://dx.doi.org/10.3390/cancers15123220] [PMID: 37370830]
[49]
Cucolo, L.; Chen, Q.; Qiu, J.; Yu, Y.; Klapholz, M.; Budinich, K.A.; Zhang, Z.; Shao, Y.; Brodsky, I.E.; Jordan, M.S.; Gilliland, D.G.; Zhang, N.R.; Shi, J.; Minn, A.J. The interferon-stimulated gene RIPK1 regulates cancer cell intrinsic and extrinsic resistance to immune checkpoint blockade. Immunity, 2022, 55(4), 671-685.e10.
[http://dx.doi.org/10.1016/j.immuni.2022.03.007] [PMID: 35417675]
[50]
Song, J.; Yang, R.; Wei, R.; Du, Y.; He, P.; Liu, X. Pan- cancer analysis reveals RIPK2 predicts prognosis and promotes immune therapy resistance via triggering cytotoxic T lymphocytes dysfunction. Mol. Med., 2022, 28(1), 47.
[http://dx.doi.org/10.1186/s10020-022-00475-8] [PMID: 35508972]
[51]
Le, D.T.; Durham, J.N.; Smith, K.N.; Wang, H.; Bartlett, B.R.; Aulakh, L.K.; Lu, S.; Kemberling, H.; Wilt, C.; Luber, B.S.; Wong, F.; Azad, N.S.; Rucki, A.A.; Laheru, D.; Donehower, R.; Zaheer, A.; Fisher, G.A.; Crocenzi, T.S.; Lee, J.J.; Greten, T.F.; Duffy, A.G.; Ciombor, K.K.; Eyring, A.D.; Lam, B.H.; Joe, A.; Kang, S.P.; Holdhoff, M.; Danilova, L.; Cope, L.; Meyer, C.; Zhou, S.; Goldberg, R.M.; Armstrong, D.K.; Bever, K.M.; Fader, A.N.; Taube, J.; Housseau, F.; Spetzler, D.; Xiao, N.; Pardoll, D.M.; Papadopoulos, N.; Kinzler, K.W.; Eshleman, J.R.; Vogelstein, B.; Anders, R.A.; Diaz, L.A., Jr Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade. Science, 2017, 357(6349), 409-413.
[http://dx.doi.org/10.1126/science.aan6733] [PMID: 28596308]
[52]
Wang, H.; Fang, L.; Jiang, J.; Kuang, Y.; Wang, B.; Shang, X.; Han, P.; Li, Y.; Liu, M.; Zhang, Z.; Li, P. The cisplatin-induced lncRNA PANDAR dictates the chemoresistance of ovarian cancer via regulating SFRS2-mediated p53 phosphorylation. Cell Death Dis., 2018, 9(11), 1103.
[http://dx.doi.org/10.1038/s41419-018-1148-y] [PMID: 30375398]
[53]
Dai, C.; Xu, P.; Liu, S.; Xu, S.; Xu, J.; Fu, Z.; Cao, J.; Lv, M.; Zhou, J.; Liu, G.; Zhang, H.; Jia, X. Long noncoding RNA ZEB1-AS1 affects paclitaxel and cisplatin resistance by regulating MMP19 in epithelial ovarian cancer cells. Arch. Gynecol. Obstet., 2021, 303(5), 1271-1281.
[http://dx.doi.org/10.1007/s00404-020-05858-y] [PMID: 33151424]
[54]
Fathi, M.; Barar, J.; Erfan-Niya, H.; Omidi, Y. Methotrexate-conjugated chitosan-grafted pH- and thermo-responsive magnetic nanoparticles for targeted therapy of ovarian cancer. Int. J. Biol. Macromol., 2020, 154, 1175-1184.
[http://dx.doi.org/10.1016/j.ijbiomac.2019.10.272] [PMID: 31730949]
[55]
Han, Z.; Shi, L. Long non-coding RNA LUCAT1 modulates methotrexate resistance in osteosarcoma via miR-200c/ABCB1 axis. Biochem. Biophys. Res. Commun., 2018, 495(1), 947-953.
[http://dx.doi.org/10.1016/j.bbrc.2017.11.121] [PMID: 29170124]
[56]
Yuan, Z.; Zhang, Y.; Cao, D.; Shen, K.; Li, Q.; Zhang, G.; Wu, X.; Cui, M.; Yue, Y.; Cheng, W.; Wang, L.; Qu, P.; Tao, G.; Hou, J.; Sun, L.; Meng, Y.; Li, G.; Li, C.; Shi, H.; Chen, Y. Pegylated liposomal doxorubicin in patients with epithelial ovarian cancer. J. Ovarian Res., 2021, 14(1), 12.
[http://dx.doi.org/10.1186/s13048-020-00736-2] [PMID: 33423683]
[57]
Chen, Q.; Yang, H.; Zhu, X.; Xiong, S.; Chi, H.; Xu, W. Integrative analysis of the doxorubicin-associated lncrna–mrna network identifies chemoresistance-associated lnc-TRDMT1-5 as a biomarker of breast cancer progression. Front. Genet., 2020, 11, 566.
[http://dx.doi.org/10.3389/fgene.2020.00566] [PMID: 32547604]
[58]
Hong, S.H.; Lee, S.; Kim, H.G.; Lee, H.J.; Jung, K.H.; Lee, S.C.; Lee, N.R.; Yun, J.; Woo, I.S.; Park, K.H.; Kim, K.; Kim, H.Y.; Rha, S.Y.; Byun, J.H. Phase II study of gemcitabine and vinorelbine as second- or third-line therapy in patients with primary refractory or platinum-resistant recurrent ovarian and primary peritoneal cancer by the Korean cancer study group (KCSG)_KCSG GY10-10. Gynecol. Oncol., 2015, 136(2), 212-217.
[http://dx.doi.org/10.1016/j.ygyno.2014.11.017] [PMID: 25462205]
[59]
Rothenberg, M.L.; Liu, P.Y.; Wilczynski, S.; Nahhas, W.A.; Winakur, G.L.; Jiang, C.S.; Moinpour, C.M.; Lyons, B.; Weiss, G.R.; Essell, J.H.; Smith, H.O.; Markman, M.; Alberts, D.S. Phase II trial of vinorelbine for relapsed ovarian cancer: A Southwest Oncology Group study. Gynecol. Oncol., 2004, 95(3), 506-512.
[http://dx.doi.org/10.1016/j.ygyno.2004.09.004] [PMID: 15581954]
[60]
Ma, J.; Fan, Z.; Tang, Q.; Xia, H.; Zhang, T.; Bi, F. Aspirin attenuates YAP and β-catenin expression by promoting β-TrCP to overcome docetaxel and vinorelbine resistance in triple-negative breast cancer. Cell Death Dis., 2020, 11(7), 530.
[http://dx.doi.org/10.1038/s41419-020-2719-2] [PMID: 32661222]
[61]
Tamari, S.; Menju, T.; Toyazaki, T.; Miyamoto, H.; Chiba, N.; Noguchi, M.; Ishikawa, H.; Miyata, R.; Kayawake, H.; Tanaka, S.; Yamada, Y.; Yutaka, Y.; Nakajima, D.; Ohsumi, A.; Hamaji, M.; Date, H. Nrf2/p-Fyn/ABCB1 axis accompanied by p-Fyn nuclear accumulation plays pivotal roles in vinorelbine resistance in non-small cell lung cancer. Oncol. Rep., 2022, 48(4), 171.
[http://dx.doi.org/10.3892/or.2022.8386] [PMID: 35959810]
[62]
Busacca, S.; O’Regan, L.; Singh, A.; Sharkey, A.J.; Dawson, A.G.; Dzialo, J.; Parsons, A.; Kumar, N.; Schunselaar, L.M.; Guppy, N.; Nakas, A.; Sheaff, M.; Mansfield, A.S.; Janes, S.M.; Baas, P.; Fry, A.M.; Fennell, D.A. BRCA1/MAD2L1 deficiency disrupts the spindle assembly checkpoint to confer vinorelbine resistance in mesothelioma. Mol. Cancer Ther., 2021, 20(2), 379-388.
[http://dx.doi.org/10.1158/1535-7163.MCT-20-0363] [PMID: 33158996]
[63]
Guan, L.Y.; Lu, Y. New developments in molecular targeted therapy of ovarian cancer. Discov. Med., 2018, 26(144), 219-229.
[PMID: 30695681]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy