https://doi.org/10.4081/ejh.2023.3570
Neurokinin-1 receptor is highly expressed in cervical cancer and its antagonist induces cervical cancer cell apoptosis
Submitted: 28 September 2022
Accepted: 28 December 2022
Published: 11 January 2023
Accepted: 28 December 2022
Abstract Views: 890
PDF: 499
HTML: 23
HTML: 23
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
Neurokinin-1 receptor (NK1R) belongs to tachykinin receptor family. Recent studies have suggested that NK1R was upregulated in cancer tissues including breast cancer, glioma and melanoma. Furthermore, NK1R antagonists have been employed to exert anti-tumor effect and promote cancer cell apoptosis. However, the role of NK1R in cervical cancer remains largely unknown. In this study, we aimed to detect the expression of NK1R in cervical cancer and evaluate the anti-tumor effects of NK1R antagonist on cervical cancer cells. We found that NK1R was highly expressed in cervical cancer tissues than in adjacent normal cervical tissues. Furthermore, by using NK1R antagonist we demonstrated that NK1R antagonist inhibited the viability and induced the apoptosis of cervical cancer cells in a dose-dependent manner, and the mechanism may be related to the inhibition of ERK activation and the regulation of apoptosis proteins Bcl-2 and BAX. In conclusion, these findings suggest that NK1R plays an oncogenic role in cervical cancer and is a promising target for cervical cancer therapy.
Halim A, Mustafa WA, Khairunizam W, Rahim HA, Sakeran H. Nucleus detection on pap smear images for cervical cancer diagnosis: A Review Analysis. Oncologie 2021;23:73-88.
DOI: https://doi.org/10.32604/Oncologie.2021.015154
Sundaram MK, Almutary AG, Haque S, Faheem SM, Arif Hussain A. Awareness of human papilloma virus and its association with cervical cancer among female university students: A study from United Arab Emirates. Oncologie 2021;23:269-77.
DOI: https://doi.org/10.32604/Oncologie.2021.016002
Gao W, Ma Q, Tang C, Zhan Y, Duan Y, Ni H, et al. Microenvironment and related genes predict outcomes of patients with cervical cancer: evidence from TCGA and bioinformatic analysis. Biocell 2020;44:597-605.
DOI: https://doi.org/10.32604/biocell.2020.011328
Liu Y, An S, Ward R, Yang Y, Guo XX, Li W, et al. G protein-coupled receptors as promising cancer targets. Cancer Lett 2016;376:226-39.
DOI: https://doi.org/10.1016/j.canlet.2016.03.031
Hauser AS, Attwood MM, Rask-Andersen M, Schiöth HB, Gloriam DE. Trends in GPCR drug discovery: new agents, targets and indications. Nat Rev Drug Disc 2017;16:829–42.
DOI: https://doi.org/10.1038/nrd.2017.178
Douglas SD, Leeman SE. Neurokinin-1 receptor: functional significance in the immune system in reference to selected infections and inflammation. Ann N Y Acad Sci 2011;1217:83-95.
DOI: https://doi.org/10.1111/j.1749-6632.2010.05826.x
Majkowska-Pilip AA-O, Halik PA-O, Gniazdowska EA-O. The significance of NK1 receptor ligands and their application in targeted radionuclide tumour therapy. Pharmaceutics 2019;11:443.
DOI: https://doi.org/10.3390/pharmaceutics11090443
Wang F, Liu S, Liu J, Feng F, Guo Y, Zhang W, et al. SP promotes cell proliferation in esophageal squamous cell carcinoma through the NK1R/Hes1 axis. Biochem Biophys Res Commun 2019;514:1210–6.
Huang C, Li Y, Guo Y, Zhang Z, Lian G, Chen Y, et al. MMP1/PAR1/SP/NK1R paracrine loop modulates early perineural invasion of pancreatic cancer cells. Theranostics 2018;8:3074-86.
DOI: https://doi.org/10.7150/thno.24281
Deng XT, Tang SM, Wu PY, Li QP, Ge XX, Xu BM, et al. SP/NK-1R promotes gall bladder cancer cell proliferation and migration. J Cell Mol Med 2019;23:7961-73.
DOI: https://doi.org/10.1111/jcmm.14230
Bayati S, Bashash D, Ahmadian S, Safaroghli-Azar A, Alimoghaddam K, Ghavamzadeh A, et al. Inhibition of tachykinin NK1 receptor using aprepitant induces apoptotic cell death and G1 arrest through Akt/p53 axis in pre-B acute lymphoblastic leukemia cells. Eur J Pharm 2016;791:274-83.
DOI: https://doi.org/10.1016/j.ejphar.2016.09.006
Javid H, Asadi J, Zahedi Avval F, Afshari AR, Hashemy SI. The role of substance P/neurokinin 1 receptor in the pathogenesis of esophageal squamous cell carcinoma through constitutively active PI3K/Akt/NF-κB signal transduction pathways. Mol Biol Rep 2020;47:2253-63.
DOI: https://doi.org/10.1007/s11033-020-05330-9
Mozafari M, Ebrahimi S, Darban RA, Hashemy SI. Potential in vitro therapeutic effects of targeting SP/NK1R system in cervical cancer. Mol Biol Rep 2022;49:1067-76.
DOI: https://doi.org/10.1007/s11033-021-06928-3
Wang F, Liu S, Liiu J, Feng F, Guo Y, Zhang W, et al. SP promotes cell proliferation in esophageal squamous cell carcinoma through the NK1R/Hes1 axis. Biochem Biophys Res Commun 2019;514:1210-6.
DOI: https://doi.org/10.1016/j.bbrc.2019.05.092
Nizam E, Erin N. Differential consequences of neurokinin receptor 1 and 2 antagonisits in metastatic breast carcinoma cells. Effects independent of substance P. Biomed Pharmacother 2018;108:263-70.
DOI: https://doi.org/10.1016/j.biopha.2018.09.013
Gharaee N, Pourali L, Jafarian AH, Hashemy SI. Evaluation of serum level of substance P and tissue distribution of NK-1 receptor in endometrial cancer. Mol Biol Rep 2018;45:2257-62.
DOI: https://doi.org/10.1007/s11033-018-4387-1
Ortiz-Prieto A, Bernabeu-Wittel J, Zulueta-Dorado T, Lorente-Lavirgen AI, Muñoz M. Immunolocalization of substance P and NK-1 receptor in vascular anomalies. Arch Dermatol Res 2017;309:97-102.
DOI: https://doi.org/10.1007/s00403-016-1707-y
Zhang L, Wang L, Dong D, Wang Z, Ji W, Yu M, et al. MiR-34b/c-5p and the neurokin-1 receptor regulate breast cancer cell proliferation and apoptosis. Cell Prolif 2019;52:e12527.
DOI: https://doi.org/10.1111/cpr.12527
Muñoz M, Rosso M, Coveñas R. The NK-1receptor antagonist L-732,138 induce apoptosis in human gastrointestinal cancer cell lines. Pharmacol Rep 2017;69:696-701.
DOI: https://doi.org/10.1016/j.pharep.2017.02.002
Nizam E, Köksoy S, Erin N. NK1R antagonist decreases inflammation and metastasis of breast carcinoma cells metastasized to liver but not to brain; phenotype-dependent therapeutic and toxic consequences. Cancer Immunol Immunother 2020;69:1639-50.
DOI: https://doi.org/10.1007/s00262-020-02574-z
Virtakoivu R, Mai A, Mattila E, De Franceschi N, Imanishi SY, Corthals G, et al. Vimentin-ERK signaling uncouples slug gene regulatory function. Cancer Res 2015,75:2349-62.
DOI: https://doi.org/10.1158/0008-5472.CAN-14-2842
Peng Y, Li W, Chen S, Wu W, Shang Z. MiR-494-3p regulates cell proliferation and apoptosis via KLF7 in Schwann cells. Biocell 2021;45:57-64.
DOI: https://doi.org/10.32604/biocell.2021.011756
Ethics Approval
This study was approved by Ethics Committee of Hebei Medical University (approval No. 2018019)Supporting Agencies
Hebei Province Medical Science Research Key Project ProgramHow to Cite
Guan, L., Yuan, S., Ma, J., Liu, H., Huang, L., & Zhang, F. (2023). Neurokinin-1 receptor is highly expressed in cervical cancer and its antagonist induces cervical cancer cell apoptosis. European Journal of Histochemistry, 67(1). https://doi.org/10.4081/ejh.2023.3570
Copyright (c) 2023 The Author(s)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
PAGEPress has chosen to apply the Creative Commons Attribution NonCommercial 4.0 International License (CC BY-NC 4.0) to all manuscripts to be published.
Similar Articles
- E. Akat, H. Arıkan, B. Göçmen, Histochemical and biometric study of the gastrointestinal system of Hyla orientalis (Bedriaga, 1890) (Anura, Hylidae) , European Journal of Histochemistry: Vol. 58 No. 4 (2014)
- A. Vetuschi, A. D'Alfonso, R. Sferra, D. Zanelli, S. Pompili, F. Patacchiola, E. Gaudio, G. Carta, Changes in muscularis propria of anterior vaginal wall in women with pelvic organ prolapse , European Journal of Histochemistry: Vol. 60 No. 1 (2016)
- Liqin Xi, Chen Wang, Pengyu Chen, Qi Yang, Ruiqi Hu, Haolin Zhang, Qiang Weng, Meiyu Xu, Expressions of IL-6, TNF-α and NF-κB in the skin of Chinese brown frog (Rana dybowskii) , European Journal of Histochemistry: Vol. 61 No. 4 (2017)
- L. Fassina, G. Magenes, A. Inzaghi, S. Palumbo, G. Allavena, C. Miracco, L. Pirtoli, M. Biggiogera, S. Comincini, AUTOCOUNTER, an ImageJ JavaScript to analyze LC3B-GFP expression dynamics in autophagy-induced astrocytoma cells , European Journal of Histochemistry: Vol. 56 No. 4 (2012)
- G. Di Guardo, Lipofuscin, lipofuscin-like pigments and autofluorescence , European Journal of Histochemistry: Vol. 59 No. 1 (2015)
- Y Jin, A Sun, S Noriki, Y Imamura, M Fukuda, Detection of cancer clones in human colorectal adenoma as revealed by increased DNA instability and other bio-markers , European Journal of Histochemistry: Vol. 51 No. 1 (2007)
- Wenjing Liu, Yongchun Zhang, Cheng Liang, Xuefang Jiang, Developmental expression of calretinin in the mouse cochlea , European Journal of Histochemistry: Vol. 68 No. 4 (2024)
- Anna Cleta Croce, Giovanni Bottiroli, Lipids: Evergreen autofluorescent biomarkers for the liver functional profiling , European Journal of Histochemistry: Vol. 61 No. 2 (2017)
- N. Kiga, I. Tojyo, T. Matsumoto, Y. Hiraishi, Y. Shinohara, S. Fujita, Expression of lumican related to CD34 and VEGF in the articular disc of the human temporomandibular joint. , European Journal of Histochemistry: Vol. 54 No. 3 (2010)
- A. Arcucci, M.R. Ruocco, F. Albano, G. Granato, V. Romano, G. Corso, C. Bancone, E. De Vendittis, A. Della Corte, S. Montagnani, Analysis of extracellular superoxide dismutase and Akt in ascending aortic aneurysm with tricuspid or bicuspid aortic valve , European Journal of Histochemistry: Vol. 58 No. 3 (2014)
<< < 24 25 26 27 28 29 30 31 32 33 > >>
You may also start an advanced similarity search for this article.
