Giampietri Claudia, Pizzichini Elisa, Somma Francesca, Petrungaro Simonetta, De Santis Elena, Rahimi Siavash, Facchiano Antonio, Fabrizi Cinzia
Department of Anatomy, Histology, Forensic Medicine and Orthopaedics, Sapienza University of Rome, 00161 Rome, Italy.
Istituto Dermopatico dell'Immacolata, IDI-IRCCS, 00167 Rome, Italy.
Int J Mol Sci. 2025 Jul 22;26(15):7064. doi: 10.3390/ijms26157064.
In recent years, a long list of relevant studies has highlighted the engagement of the nervous system in the fine-tuning of tumor development and progression. Several authors have shown that different types of nerve fibres (sympathetic, parasympathetic/vagal or somatosensory fibres) may contribute to tumor innervation affecting cancer initiation, progression and metastasis. A large presence of nerve fibres is frequently observed in tumors with respect to the corresponding healthy tissues. In this regard, it is worth noting that in some cases a reduced innervation may associate with slow tumor growth in a tissue-specific manner. Current studies have begun to shed light over the role played in this specific process by Schwann cells (SCs), the most abundant glial cells of the peripheral nervous system. SCs observed in cancer tissues share strong similarities with repair SCs that appear after nerve injury. A large body of research indicates that SCs may have a role in shaping the microenvironment of tumors by regulating the immune response and influencing their invasiveness. In this review, we summarize data relevant to the role of peripheral innervation in general, and of SCs in particular, in defining the progression of different tumors: melanoma that originate in the skin with mainly sensory innervation; pancreatic and liver-derived tumors (e.g., pancreatic adenocarcinoma and cholangiocarcinoma) with mainly autonomous innervation. We conclude by summarizing data regarding hepatocarcinoma (with anatomical predominance of small autonomic nerve fibres) in which the potential relationship between innervation and tumor progression has been little explored, and largely remains to be defined.
近年来,一系列相关研究强调了神经系统在肿瘤发生发展的精细调节中的作用。多位作者表明,不同类型的神经纤维(交感神经、副交感神经/迷走神经或躯体感觉神经纤维)可能参与肿瘤神经支配,影响癌症的起始、进展和转移。与相应的健康组织相比,肿瘤中经常观察到大量神经纤维。在这方面,值得注意的是,在某些情况下,神经支配减少可能以组织特异性方式与肿瘤生长缓慢相关。目前的研究已经开始揭示施万细胞(SCs)在这一特定过程中所起的作用,施万细胞是周围神经系统中最丰富的神经胶质细胞。在癌组织中观察到的施万细胞与神经损伤后出现的修复性施万细胞有很强的相似性。大量研究表明,施万细胞可能通过调节免疫反应和影响肿瘤的侵袭性,在塑造肿瘤微环境中发挥作用。在这篇综述中,我们总结了与周围神经支配,特别是施万细胞在定义不同肿瘤进展中的作用相关的数据:主要起源于具有感觉神经支配的皮肤的黑色素瘤;主要具有自主神经支配的胰腺和肝脏来源的肿瘤(如胰腺腺癌和胆管癌)。我们通过总结关于肝癌(以小的自主神经纤维在解剖学上占优势)的数据来得出结论,其中神经支配与肿瘤进展之间的潜在关系很少被探索,并且在很大程度上仍有待确定。