卵巢癌症免疫治疗途径:IL9抑制卵巢癌症生长及上调Ox40L和4-1BBL表达

IF 0.5 4区 医学 Q4 OBSTETRICS & GYNECOLOGY
Erin C. Kaser, Marco Lequio, Ziwen Zhu, Zachary E. Hunzeker, Aidan J. Heslin, Kyle P. D’mello, HuaPing Xiao, Qian Bai, M. Wakefield, Yujiang Fang
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引用次数: 1

摘要

目的:癌症是妇科恶性肿瘤中最致命的一种。目前的治疗方法包括化疗减瘤手术,但即使进行了治疗,五年生存率也低于45%。癌症免疫疗法是一种正在高度研究的创新治疗方案。白细胞介素(IL)是人类免疫系统用来帮助检测和破坏癌症细胞的信号分子。肿瘤细胞逃避免疫系统的能力是我们在对抗癌症时面临的主要挑战。Ox40L/Ox40和4-1BBL/4-1BB是增加T细胞激活以消除肿瘤的关键免疫共刺激分子。过去的研究表明,IL9对各种类型的癌症具有独特的影响,但其在癌症中的作用尚未得到评估。在本研究中,用IL9处理卵巢癌症细胞,并测定Ox40L和4-1BBL的表达。方法:应用IL9对癌症A2780细胞进行治疗。卵巢癌症细胞的增殖通过克隆原性生存测定法和快速增殖测定法测定。进行RT-PCR以确定IL9是否上调共刺激分子Ox40L和4-1BBL。进行IHC以进一步研究IL9对Ox40L和4-1BBL的上调。结果:用IL9治疗A2780卵巢癌症细胞,可降低卵巢癌症细胞的增殖。通过使用RT-PCR,确定IL9处理的卵巢癌症细胞显示出共刺激分子Ox40L和4-1BBL的上调。IHC进一步证实OX40L和4-1BBL的上调。结论:IL9抑制卵巢癌症细胞生长,上调关键免疫共刺激分子Ox40L和4-1BBL。这表明Ox40L和4-1BBL表达的增加可能与IL9对卵巢癌症增殖的抑制作用有关。本研究为进一步研究Ox40L和4-1BBL在卵巢癌症生长中的作用提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ovarian Cancer Immunotherapy en Route: IL9 Inhibits Growth of Ovarian Cancer and Upregulates its Expression of Ox40L and 4-1BBL
Objective : Ovarian cancer is the deadliest of all gynecologic tumors. Current treatment methods include debulking surgery with chemotherapy, however even with treatment, the five-year survival rate is below 45%. Cancer immunotherapy is an innovative treatment option being highly researched. Interleukins (ILs) are signaling molecules used by the human immune system to assist in detecting and destroying cancer cells. The ability of tumor cells to evade the immune system is a major challenge we face in fighting cancer. Ox40L/Ox40 and 4-1BBL/4-1BB are key immune costimulatory molecules that increase T cell activation to eliminate tumors. Past research has shown that IL9 has unique influences on various types of cancer, however, its role in ovarian cancer has not yet been assessed. In this study, ovarian cancer cells were treated with IL9 and the expression of Ox40L and 4-1BBL were measured. Methods : A2780 ovarian cancer cells were treated with IL9. Proliferation of ovarian cancer cells was measured by a Clonogenic Survival Assay and Quick Proliferation Assay. RT-PCR was conducted to determine whether IL9 upregulated the costimulatory molecules Ox40L and 4-1BBL. IHC was performed to further investigate IL9 upregulation of Ox40L and 4-1BBL. Results : Treatment of A2780 ovarian cancer cells with IL9 resulted in decreased proliferation of the ovarian cancer cells. By using RT-PCR, it was determined that IL9 treated ovarian cancer cells displayed upregulation of the costimulatory molecules Ox40L and 4-1BBL. Upregulation of OX40L and 4-1BBL was further confirmed by IHC. Conclusions : IL9 inhibited growth of ovarian cancer cells, and IL9 upregulated the key immune costimulatory molecules Ox40L and 4-1BBL. This suggests that increased expression of Ox40L and 4-1BBL may be associated with the inhibitory effect of IL9 on proliferation of ovarian cancer. This study warrants further investigation of the role of Ox40L and 4-1BBL in ovarian cancer growth.
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来源期刊
自引率
25.00%
发文量
58
审稿时长
1 months
期刊介绍: EJGO is dedicated to publishing editorial articles in the Distinguished Expert Series and original research papers, case reports, letters to the Editor, book reviews, and newsletters. The Journal was founded in 1980 the second gynaecologic oncology hyperspecialization Journal in the world. Its aim is the diffusion of scientific, clinical and practical progress, and knowledge in female neoplastic diseases in an interdisciplinary approach among gynaecologists, oncologists, radiotherapists, surgeons, chemotherapists, pathologists, epidemiologists, and so on.
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