Nara Medical University, Department of Urology, Nara, Japan.
University of Hawaii Cancer Center, Clinical and Translational Research, Honolulu, Hawaii.
Theranostics. 2019 Jan 25;9(3):853-867. doi: 10.7150/thno.29553. eCollection 2019.
: The expression of the chemokine (C-X-C motif) ligand 1 (CXCL1), an inflammatory protein, has been reported to be up-regulated in many human cancers. The mechanisms through which aberrant cellular CXCL1 levels promote specific steps in tumor growth and progression are unknown. : We described the anticancer effects and mechanism of action of HL2401, a monoclonal antibody directed at CXCL1 with and data on bladder and prostate cancers. : HL2401 inhibited proliferation and invasion of bladder and prostate cells along with disrupting endothelial sprouting . Furthermore, novel mechanistic investigations revealed that CXCL1 expression stimulated interleukin 6 (IL6) expression and repressed tissue inhibitor of metalloproteinase 4 (TIMP4). Systemic administration of HL2401 in mice bearing bladder and prostate xenograft tumors retarded tumor growth through the inhibition of cellular proliferation and angiogenesis along with an induction of apoptosis. Our findings reveal a previously undocumented relationship between CXCL1, IL6 and TIMP4 in solid tumor biology. : Taken together, our results argue that CXCL1 plays an important role in sustaining the growth of bladder and prostate tumors via up-regulation of IL6 and down-regulation of TIMP4. Targeting these critical interactions with a CXCL1 monoclonal antibody offers a novel strategy to therapeutically manage bladder and prostate cancers.
趋化因子(C-X-C 基序)配体 1(CXCL1)的表达已被报道在许多人类癌症中上调。细胞 CXCL1 水平异常升高促进肿瘤生长和进展特定步骤的机制尚不清楚。
我们描述了 HL2401 的抗癌作用和作用机制,HL2401 是一种针对 CXCL1 的单克隆抗体,具有 和 数据的膀胱癌和前列腺癌。
HL2401 抑制膀胱和前列腺细胞的增殖和侵袭,同时破坏内皮细胞发芽。此外,新的机制研究表明,CXCL1 表达刺激白细胞介素 6(IL6)表达并抑制组织金属蛋白酶抑制剂 4(TIMP4)。HL2401 在携带膀胱和前列腺异种移植肿瘤的小鼠中的系统给药通过抑制细胞增殖和血管生成以及诱导细胞凋亡来延缓肿瘤生长。我们的发现揭示了 CXCL1、IL6 和 TIMP4 在实体瘤生物学中以前未被记录的关系。
综上所述,我们的结果表明,CXCL1 通过上调 IL6 和下调 TIMP4 在维持膀胱和前列腺肿瘤的生长中发挥重要作用。用 CXCL1 单克隆抗体靶向这些关键相互作用为治疗性管理膀胱癌和前列腺癌提供了一种新策略。