The clinicopathological and prognostic significance of autonomic nerves in salivary duct carcinoma.

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-09-01 Epub Date: 2024-07-23 DOI:10.1007/s00428-024-03873-x
Manami Kajiwara, Hideaki Takahashi, Masato Nakaguro, Daisuke Kawakita, Hideaki Hirai, Yoshitaka Utsumi, Makoto Urano, Yukiko Sato, Kiyoaki Tsukahara, Satoshi Kano, Kenji Okami, Hiroyuki Ozawa, Keisuke Yamazaki, Takuro Okada, Akira Shimizu, Kenji Hanyu, Akihiro Sakai, Mayu Yamauchi, Mariko Sekimizu, Toyoyuki Hanazawa, Yuki Saito, Yushi Ueki, Yoshitaka Honma, Tomoyuki Arai, Sho Iwaki, Koji Yamamura, Yorihisa Imanishi, Yuichiro Sato, Yuichiro Tada, Toshitaka Nagao
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Abstract

Many researchers have focused on the role of the autonomic nervous system in the tumor microenvironment. Autonomic nerves include the sympathetic and parasympathetic nerves, which are known to induce cancer growth and metastasis. However, in salivary duct carcinoma (SDC), a rare and highly malignant tumor, the issue should be investigated from both biological and therapeutic perspectives. We explored the clinicopathological and prognostic implications of the autonomic nerves in 129 SDCs. Immunohistochemistry was performed to determine the nature of each nerve using antibodies against S100, tyrosine hydroxylase (TH) as a sympathetic marker, and vesicular acetylcholine transporter (VAChT) as a parasympathetic marker. The area of each marker-positive nerve was digitized and evaluated quantitatively. Double immunofluorescence for TH and VAChT was performed in selected cases. The expression of the secreted neurotrophins was also examined. S100-positive nerves were present in the cancer tissue in 94 of 129 cases (72.9%). Among them, TH-positive sympathetic nerves and/or VAChT-positive parasympathetic nerves were identified in 92 cases (97.9%), and 59 cases (62.8%) had TH/VAChT-co-expressing nerves. Double immunofluorescence revealed a mosaic pattern of sympathetic and parasympathetic fibers in co-expressing nerve bundles. The presence of autonomic nerves, regardless of their area, was significantly associated with aggressive histological features, advanced T/N classification, and a poor prognosis, with shorter disease-free and overall survival. There was an association between some tumor immune microenvironment-related markers and the autonomic nerve status, but not the latter and the secreted neurotrophin expression. This study suggests that autonomic nerves might play a role in the progression of SDC.

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涎管癌自律神经的临床病理和预后意义。
许多研究人员都在关注自主神经系统在肿瘤微环境中的作用。自主神经包括交感神经和副交感神经,众所周知,交感神经和副交感神经可诱导癌症生长和转移。然而,唾液腺导管癌(SDC)是一种罕见的高度恶性肿瘤,应从生物学和治疗学两个角度研究这一问题。我们对 129 例 SDC 中自律神经的临床病理和预后影响进行了探讨。我们使用 S100、作为交感神经标记的酪氨酸羟化酶(TH)和作为副交感神经标记的囊泡乙酰胆碱转运体(VAChT)抗体进行了免疫组化,以确定每条神经的性质。对每个标记阳性神经的面积进行数字化和定量评估。对部分病例进行了 TH 和 VAChT 的双重免疫荧光检测。还检测了分泌型神经营养素的表达。129 个病例中有 94 个(72.9%)癌症组织中存在 S100 阳性神经。其中,92 例(97.9%)发现了 TH 阳性交感神经和/或 VAChT 阳性副交感神经,59 例(62.8%)发现了 TH/VAChT 共同表达神经。双重免疫荧光显示,在共同表达的神经束中,交感神经和副交感神经纤维呈镶嵌图案。自律神经的存在(无论其面积大小)与侵袭性组织学特征、晚期T/N分类和预后不良(无病生存期和总生存期较短)显著相关。一些肿瘤免疫微环境相关标记物与自主神经状态有关,但后者与分泌性神经营养素的表达无关。这项研究表明,自主神经可能在SDC的进展过程中发挥作用。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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