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Cited by in CrossRef
For: Lü SH, Zhou Y, Que HP, Liu SJ. Peptidergic innervation of human esophageal and cardiac carcinoma. World J Gastroenterol 2003; 9(3): 399-403 [PMID: 12632484 DOI: 10.3748/wjg.v9.i3.399]
URL: https://www.wjgnet.com/1007-9327/full/v9/i3/399.htm
Number Citing Articles
1
Janusz Godlewski, Zenon Pidsudko. Characteristic of galaninergic components of the enteric nervous system in the cancer invasion of human large intestineAnnals of Anatomy - Anatomischer Anzeiger 2012; 194(4): 368 doi: 10.1016/j.aanat.2011.11.009
2
Zhi Jie Li, Chi Hin Cho. Neurotransmitters, more than meets the eye — Neurotransmitters and their perspectives in cancer development and therapyEuropean Journal of Pharmacology 2011; 667(1-3): 17 doi: 10.1016/j.ejphar.2011.05.077
3
James H. Baraldi, German V. Martyn, Galina V. Shurin, Michael R. Shurin. Tumor Innervation: History, Methodologies, and SignificanceCancers 2022; 14(8): 1979 doi: 10.3390/cancers14081979
4
Mario Mancino, Elisabet Ametller, Pedro Gascón, Vanessa Almendro. The neuronal influence on tumor progressionBiochimica et Biophysica Acta (BBA) - Reviews on Cancer 2011; 1816(2): 105 doi: 10.1016/j.bbcan.2011.04.005
5
Zodwa Dlamini, Kgomotso Mathabe, Llewellyn Padayachy, Rahaba Marima, George Evangelou, Konstantinos N. Syrigos, Arianna Bianchi, Georgios Lolas, Rodney Hull. Many Voices in a Choir: Tumor-Induced Neurogenesis and Neuronal Driven Alternative Splicing Sound Like Suspects in Tumor Growth and DisseminationCancers 2021; 13(9): 2138 doi: 10.3390/cancers13092138
6
Antonino Amoddeo. Mathematical Model and Numerical Simulation for Electric Field Induced Cancer Cell MigrationMathematical and Computational Applications 2020; 26(1): 4 doi: 10.3390/mca26010004
7
Melanie J Voss, Frank Entschladen. Tumor interactions with soluble factors and the nervous systemCell Communication and Signaling 2010; 8(1) doi: 10.1186/1478-811X-8-21
8
Hideyo Miyato, Joji Kitayama, Hironori Ishigami, Shoichi Kaisaki, Hirokazu Nagawa. Loss of Sympathetic Nerve Fibers Around Intratumoral Arterioles Reflects Malignant Potential of Gastric CancerAnnals of Surgical Oncology 2011; 18(8): 2281 doi: 10.1245/s10434-011-1562-1
9
Karla V. Torres-Juárez, Felisbina Luisa Queiroga, Laura P. Romero-Romero. The Nervous System as a Regulator of Cancer Hallmarks: Insights into Therapeutic ImplicationsCancers 2022; 14(18): 4372 doi: 10.3390/cancers14184372
10
Roberta Colucci, Silvia Moretti. The role of stress and beta-adrenergic system in melanoma: current knowledge and possible therapeutic optionsJournal of Cancer Research and Clinical Oncology 2016; 142(5): 1021 doi: 10.1007/s00432-015-2078-z
11
Kerstin Lang, Frank Entschladen, Corinna Weidt, Kurt S. Zaenker. Tumor immune escape mechanisms: impact of the neuroendocrine systemCancer Immunology, Immunotherapy 2006; 55(7): 749 doi: 10.1007/s00262-006-0126-x
12
Frank Entschladen, Theodore L Drell, Kerstin Lang, Jan Joseph, Kurt S Zaenker. Tumour-cell migration, invasion, and metastasis: navigation by neurotransmittersThe Lancet Oncology 2004; 5(4): 254 doi: 10.1016/S1470-2045(04)01431-7
13
SHA LI, YANLAI SUN, DONGWEI GAO. Role of the nervous system in cancer metastasisOncology Letters 2013; 5(4): 1101 doi: 10.3892/ol.2013.1168
14
Hannah P. Priyanka, Rahul S. Nair, Sanjana Kumaraguru, Kirtikesav Saravanaraj, Vasantharekha Ramasamy. Insights on neuroendocrine regulation of immune mediators in female reproductive aging and cancerAIMS Molecular Science 2021; 8(2): 127 doi: 10.3934/molsci.2021010
15
Jie Li, Mengjie Che, Bin Zhang, Kewei Zhao, Chao Wan, Kunyu Yang. The association between the neuroendocrine system and the tumor immune microenvironment: Emerging directions for cancer immunotherapyBiochimica et Biophysica Acta (BBA) - Reviews on Cancer 2023; 1878(6): 189007 doi: 10.1016/j.bbcan.2023.189007
16
Melanie J Voss, Bernd Niggemann, Kurt S Zänker, Frank Entschladen. PC-3 prostate carcinoma cells release signal substances that influence the migratory activity of cells in the tumor's microenvironmentCell Communication and Signaling 2010; 8(1) doi: 10.1186/1478-811X-8-17
17
Georgios Lolas, Arianna Bianchi, Konstantinos N. Syrigos. Tumour-induced neoneurogenesis and perineural tumour growth: a mathematical approachScientific Reports 2016; 6(1) doi: 10.1038/srep20684
18
Sharif Shalabi, Ali Belayachi, Bruno Larrivée. Involvement of neuronal factors in tumor angiogenesis and the shaping of the cancer microenvironmentFrontiers in Immunology 2024; 15 doi: 10.3389/fimmu.2024.1284629
19
Manuel Lisardo Sánchez, Rafael Coveñas. The Galaninergic System: A Target for Cancer TreatmentCancers 2022; 14(15): 3755 doi: 10.3390/cancers14153755
20
Qianqian Zhao, Yan Yang, Xizi Liang, Guangye Du, Liwei Liu, Lingjuan Lu, Junbo Dong, Hongxiu Han, Guohua Zhang. The clinicopathological significance of neurogenesis in breast cancerBMC Cancer 2014; 14(1) doi: 10.1186/1471-2407-14-484
21
Frank Entschladen, Daniel Palm, Bernd Niggemann, Kurt S. Zaenker. The cancer's nervous tooth: Considering the neuronal crosstalk within tumorsSeminars in Cancer Biology 2008; 18(3): 171 doi: 10.1016/j.semcancer.2007.12.004
22
Janusz Godlewski, Ireneusz Mirosław Łakomy. Changes in vasoactive intestinal peptide, pituitary adenylate cyclase-activating polypeptide and neuropeptide Y-ergic structures of the enteric nervous system in the carcinoma of the human large intestine.Folia Histochemica et Cytobiologica 2010; 48(2) doi: 10.2478/v10042-010-0052-9
23
Yuri L. Bunimovich, Anton A. Keskinov, Galina V. Shurin, Michael R. Shurin. Schwann cells: a new player in the tumor microenvironmentCancer Immunology, Immunotherapy 2017; 66(8): 959 doi: 10.1007/s00262-016-1929-z
24
T. Crosson, K. Roversi, M. Balood, R. Othman, M. Ahmadi, J.‐C. Wang, P. J. Seadi Pereira, M. Tabatabaei, R. Couture, T. Eichwald, A. Latini, R.D. Prediger, M. Rangachari, C. R. Seehus, S. L. Foster, S. Talbot. Profiling of how nociceptor neurons detect danger – new and old foesJournal of Internal Medicine 2019; 286(3): 268 doi: 10.1111/joim.12957
25
Jiaqiang Dong, Fan Feng, Guanghui Xu, Hongwei Zhang, Liu Hong, Jianjun Yang. Elevated SP/NK-1R in esophageal carcinoma promotes esophageal carcinoma cell proliferation and migrationGene 2015; 560(2): 205 doi: 10.1016/j.gene.2015.02.002
26
Anton A. Keskinov, Victor Tapias, Simon C. Watkins, Yang Ma, Michael R. Shurin, Galina V. Shurin, Suzie Chen. Impact of the Sensory Neurons on Melanoma Growth In VivoPLOS ONE 2016; 11(5): e0156095 doi: 10.1371/journal.pone.0156095
27
Nathan Griffin, Christopher W. Rowe, Fangfang Gao, Phillip Jobling, Vanessa Wills, Marjorie M. Walker, Sam Faulkner, Hubert Hondermarck. Clinicopathological Significance of Nerves in Esophageal CancerThe American Journal of Pathology 2020; 190(9): 1921 doi: 10.1016/j.ajpath.2020.05.012
28
Ivan H. Vachkov, Xiaoyong Huang, Yoshihiro Yamada, Anton B. Tonchev, Tetsumori Yamashima, Satoru Kato, Nobuyuki Takakura. Inhibition of axonal outgrowth in the tumor environment: Involvement of class 3 semaphorinsCancer Science 2007; 98(8): 1192 doi: 10.1111/j.1349-7006.2007.00508.x
29
Aping Yuan, Jinzhong Liu, Yiqing Liu, Guanglin Cui. Chromogranin A-positive tumor cells in human esophageal squamous cell carcinomasPathology & Oncology Research 2007; 13(4): 321 doi: 10.1007/BF02940311
30
Janusz Godlewski, Jerzy Kaleczyc. Somatostatin, substance P and calcitonin gene-related peptide-positive intramural nerve structures of the human large intestine affected by carcinoma.Folia Histochemica et Cytobiologica 2010; 48(3) doi: 10.2478/v10042-010-0079-y
31
Tanya Miladinovic, Gurmit Singh. Oncodynamics: Effects of Cancer Cells on the Body2016; : 55 doi: 10.1007/978-3-319-28558-0_3
32
Daniel Albo, Catherine L. Akay, Christy L. Marshall, Jonathan A. Wilks, Gordana Verstovsek, Hao Liu, Neeti Agarwal, David H. Berger, Gustavo E. Ayala. Neurogenesis in colorectal cancer is a marker of aggressive tumor behavior and poor outcomesCancer 2011; 117(21): 4834 doi: 10.1002/cncr.26117