[1] Svennerholm L.Chromatographic Separation Of Human Brain Gangliosides[J]. J Neurochem, 1963, 10: 613-623. [2] Liu J, Zheng X, Pang X, et al.Ganglioside GD3 synthase (GD3S), a novel cancer drug target[J]. Acta Pharm Sin B, 2018, 8(5): 713-720. [3] 杨柳, 李本尚, 陈静. 以神经节苷脂GD2为靶点细胞免疫治疗神经母细胞瘤的研究进展[J]. 中华儿科杂志, 2016, 54(6): 476-478. [4] Mokbel K.GD2 in Breast Cancer: A Potential Biomarker and Therapeutic Target[J]. Cancer Genomics Proteomics, 2024, 21(6): 549-556. [5] Groux-Degroote S, Guérardel Y, Delannoy P.Gangliosides: Structures, Biosynthesis, Analysis, and Roles in Cancer[J]. Chembiochem, 2017, 18(13): 1146-1154. [6] Wei X, Li S, Wang Y.Expression of GD2 and GD3 in peripheral neuroblastic tumors[J]. Indian J Pathol Microbiol, 2025, 68(1):17-22 [7] Imamura A, Ando H, Ishida H.Chemical Synthesis of Gangliosides[J]. Methods Mol Biol, 2023, 2613: 89-100. [8] Tibbetts R, Yeo KK, Muthugounder S, et al.Anti-disialoganglioside antibody internalization by neuroblastoma cells as a mechanism of immunotherapy resistance[J]. Cancer Immunol Immunother, 2022, 71(1): 153-164. [9] Pershina O, Ermakova N, Pakhomova A, et al.Cancer Stem Cells and Somatic Stem Cells as Potential New Drug Targets, Prognosis Markers, and Therapy Efficacy Predictors in Breast Cancer Treatment[J]. Biomedicines, 2021, 9(9): 1223. [10] Shah MA, Shitara K, Lordick F, et al. Randomized, Double-Blind, Placebo-Controlled Phase III Study of Paclitaxel ± Napabucasin in Pretreated Advanced Gastric or Gastroesophageal Junction Adenocarcinoma[J]. Clin Cancer Res, 2022, 28(17): of1-of9. [11] Romaniuk-Drapa?a A, Totoń E, Taube M, et al. Breast Cancer Stem Cells and Tumor Heterogeneity: Characteristics and Therapeutic Strategies[J]. Cancers (Basel), 2024, 16(13): 2481. [12] Li W, Ma H, Zhang J, et al.Unraveling the roles of CD44/CD24 and ALDH1 as cancer stem cell markers in tumorigenesis and metastasis[J]. Sci Rep, 2017, 7(1): 13856. [13] Ordaz-Ramos A, Tellez-Jimenez O, Vazquez-Santillan K.Signaling pathways governing the maintenance of breast cancer stem cells and their therapeutic implications[J]. Front Cell Dev Biol, 2023, 11: 1221175. [14] Flores-Huerta N, Silva-CázaresMB, Arriaga-PizanoLA, et al. LncRNAs and microRNAs as Essential Regulators of Stemness in Breast Cancer Stem Cells[J]. Biomolecules, 2021, 11(3): 380. [15] Zheng Q, Zhang M, Zhou F, et al.The Breast Cancer Stem Cells Traits and Drug Resistance[J]. Front Pharmacol, 2020, 11: 599965. [16] ElbaiomyMA, Akl T, Atwan N, et al. Clinical Impact of Breast Cancer Stem Cells in Metastatic Breast Cancer Patients[J]. J Oncol, 2020, 2020: 2561726. [17] Salvadori G, Zanardi F, Iannelli F, et al. Fasting-mimicking diet blocks triple-negative breast cancer and cancer stem cell escape[J]. Cell Metab, 2021, 33(11): 2247-2259. e6. [18] BattulaVL, Shi Y, Evans KW, et al. Ganglioside GD2 identifies breast cancer stem cells and promotes tumorigenesis[J]. J Clin Invest, 2012, 122(6): 2066-2078. [19] Nguyen K, Battula VL.Targeting NFκB signaling in GD2(+) BCSCs[J]. Aging (Albany NY), 2017, 9(8): 1847-1848. [20] Corti C, Venetis K, Sajjadi E, et al.CAR-T cell therapy for triple-negative breast cancer and other solid tumors: preclinical and clinical progress[J]. Expert Opin Investig Drugs, 2022, 31(6): 593-605. [21] 齐倩, 郝辉, 徐伟, 等. 神经节苷脂GD2对人三阴性乳腺癌细胞增殖和凋亡的影响[J]. 解剖科学进展, 2024, 30(06): 614-616. [22] Liang YJ, Wang CY, Wang IA, et al.Interaction of glycosphingolipids GD3 and GD2 with growth factor receptors maintains breast cancer stem cell phenotype[J]. Oncotarget, 2017, 8(29): 47454-47473. [23] Zhang L, Chen W, Liu S, et al.Targeting Breast Cancer Stem Cells[J]. Int J Biol Sci, 2023, 19(2): 552-570. [24] Ly S, Anand V, El-Dana F, et al.Anti-GD2 antibody dinutuximab inhibits triple-negative breast tumor growth by targeting GD2(+) breast cancer stem-like cells[J]. J Immunother Cancer, 2021, 9(3): e001197. [25] Obidiro O, Battogtokh G, Akala EO.Triple Negative Breast Cancer Treatment Options and Limitations: Future Outlook[J]. Pharmaceutics, 2023, 15(7): 1796. [26] Erber R, Kailayangiri S, Huebner H, et al.Variable Expression of the Disialoganglioside GD2 in Breast Cancer Molecular Subtypes[J]. Cancers (Basel), 2021, 13(21): 5577. [27] Higashi C, Saito K, Kozuka Y, et al.Ganglioside GD2 Expression Is Associated With Unfavorable Prognosis in Early Triple-negative Breast Cancer[J]. Anticancer Res, 2023, 43(9): 4045-4053. [28] Tarantino P, Corti C, Schmid P, et al.Immunotherapy for early triple negative breast cancer: research agenda for the next decade[J]. NPJ Breast Cancer, 2022, 8(1): 23. [29] Sajjadi E, Venetis K, Scatena C, et al.Biomarkers for precision immunotherapy in the metastatic setting: hope or reality?[J]. Ecancermedicalscience, 2020, 14: 1150. [30] Geng P, Chi Y, Yuan Y, et al.Novel chimeric antigen receptor T cell-based immunotherapy: a perspective for triple-negative breast cancer[J]. Front Cell Dev Biol, 2023, 11: 1158539. [31] Gargett T, Truong NTH, Gardam B, et al.Safety and biological outcomes following a phase 1 trial of GD2-specific CAR-T cells in patients with GD2-positive metastatic melanoma and other solid cancers[J]. J Immunother Cancer, 2024, 12(5):e008659. [32] Seitz CM, Schroeder S, Knopf P, et al.GD2-targeted chimeric antigen receptor T cells prevent metastasis formation by elimination of breast cancer stem-like cells[J]. Oncoimmunology, 2020, 9(1): 1683345. [33] Philippova J, Shevchenko J, Sennikov S.GD2-targeting therapy: a comparative analysis of approaches and promising directions[J]. Front Immunol, 2024, 15: 1371345. |