A novel semi-quantitative scoring method for CD8+ tumor-infiltrating lymphocytes based on infiltration sites in gastric cancer.

IF 3.6 3区 医学 Q2 ONCOLOGY
American journal of cancer research Pub Date : 2024-12-25 eCollection Date: 2024-01-01 DOI:10.62347/JKCU5881
Yudai Nakabayashi, Jun Kiuchi, Takeshi Kubota, Takuma Ohashi, Keiji Nishibeppu, Taisuke Imamura, Kenji Nanishi, Hiroki Shimizu, Tomohiro Arita, Yusuke Yamamoto, Hirotaka Konishi, Ryo Morimura, Shuhei Komatsu, Atsushi Shiozaki, Hisashi Ikoma, Yoshiaki Kuriu, Hitoshi Fujiwara, Hitoshi Tsuda, Eigo Otsuji
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引用次数: 0

Abstract

No established method currently exists for evaluating tumor-infiltrating lymphocytes (TILs) in gastric cancer (GC), and their clinical significance based on infiltration site in GC remains unclear. In this study, we developed a method to evaluate TILs according to their infiltration site as a prognostic marker for GC. We retrospectively analyzed 103 patients with advanced GC who underwent curative resection. TILs located at the invasive margin (TILIM) and the center of tumors (TILCT) were scored semi-quantitatively using immunohistochemical staining of CD8+ T cells. The sum of the TILIM and TILCT scores was defined as the TILs score. Based on this score, patients were classified into low and high TILs groups. Quantitative TILs were also assessed to validate the semi-quantitative scoring method. Furthermore, we confirmed a tumor suppressive effect due to CD8+ T cells co-cultured in GC cell lines in vitro. In the univariate analysis, patients with low TILIM were significantly more likely to be female, younger, and have undifferentiated histological types and deeper tumor invasion compared to those with high TILIM. Similarly, patients with low TILCT had significantly more positive lymph node metastases than those with high TILCT. In the multivariate analysis, deeper tumor invasion and positive lymph node metastasis were identified as independent risk factors for patients with low TILIM and low TILCT, respectively. According to our semi-quantitative TILs scoring method, the low TILs group had significantly poorer prognoses compared to the high TILs group. This group had significantly larger tumor diameters, deeper tumor invasion, and more positive lymph node metastases. Additionally, deeper tumor invasion was an independent risk factor for the low TILs group. Quantitative TILs analysis revealed that the low TILs group had significantly lower TIL levels compared to the high TILs group. In vitro, CD8+ T cells induced apoptosis in GC cells in a concentration-dependent manner. Furthermore, these cells significantly suppressed the proliferative, migratory, and invasive capacities of GC cells. Our simple and versatile semi-quantitative scoring method for CD8+ TILs indicates that CD8+ TILs are sensitive prognostic markers. The low TILs group accurately reflects the low quantitative TIL levels and is associated with poor oncological prognosis.

基于胃癌浸润部位的CD8+肿瘤浸润淋巴细胞半定量评分新方法
胃癌(GC)中肿瘤浸润淋巴细胞(tumor-浸润淋巴细胞,til)的评价目前尚无确定的方法,其基于胃癌浸润部位的临床意义尚不清楚。在这项研究中,我们开发了一种根据浸润部位来评估TILs的方法,作为胃癌的预后标志物。我们回顾性分析了103例行根治性切除的晚期胃癌患者。采用CD8+ T细胞免疫组化染色对浸润边缘(TILIM)和肿瘤中心(TILCT)的TILs进行半定量评分。tilm和TILCT分数之和定义为TILs分数。根据该评分将患者分为TILs低组和TILs高组。定量TILs也进行了评估,以验证半定量评分方法。此外,我们证实了CD8+ T细胞在体外GC细胞系中共培养的肿瘤抑制作用。在单变量分析中,与高TILIM患者相比,低TILIM患者明显更可能是女性、年轻、未分化的组织学类型和更深的肿瘤侵袭。同样,低TILCT患者比高TILCT患者有更多的淋巴结转移阳性。在多因素分析中,较深的肿瘤侵袭和淋巴结转移阳性分别被确定为低tilm和低TILCT患者的独立危险因素。根据我们的半定量TILs评分方法,低TILs组的预后明显差于高TILs组。本组肿瘤直径明显增大,肿瘤浸润深度明显加深,淋巴结转移阳性较多。此外,较深的肿瘤浸润是低TILs组的独立危险因素。定量TILs分析显示,低TILs组的TIL水平明显低于高TILs组。体外CD8+ T细胞诱导GC细胞凋亡呈浓度依赖性。此外,这些细胞显著抑制GC细胞的增殖、迁移和侵袭能力。我们对CD8+ TILs的简单而通用的半定量评分方法表明CD8+ TILs是敏感的预后指标。低TIL组准确反映了低定量TIL水平,与肿瘤预后差有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
3.80%
发文量
263
期刊介绍: The American Journal of Cancer Research (AJCR) (ISSN 2156-6976), is an independent open access, online only journal to facilitate rapid dissemination of novel discoveries in basic science and treatment of cancer. It was founded by a group of scientists for cancer research and clinical academic oncologists from around the world, who are devoted to the promotion and advancement of our understanding of the cancer and its treatment. The scope of AJCR is intended to encompass that of multi-disciplinary researchers from any scientific discipline where the primary focus of the research is to increase and integrate knowledge about etiology and molecular mechanisms of carcinogenesis with the ultimate aim of advancing the cure and prevention of this increasingly devastating disease. To achieve these aims AJCR will publish review articles, original articles and new techniques in cancer research and therapy. It will also publish hypothesis, case reports and letter to the editor. Unlike most other open access online journals, AJCR will keep most of the traditional features of paper print that we are all familiar with, such as continuous volume, issue numbers, as well as continuous page numbers to retain our comfortable familiarity towards an academic journal.
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