Early Evaluation of Minor Serous Gland Injuries Following Fractionated Radiotherapy for Head and Neck Cancer (Immunohistochemical Study)
Mashael S Al-Qahtani1, Sherif S Hassan1,2*, and Ibraheem K Bamaga1
11Department of Basic and Clinical Oral Sciences, Faculty of Dental Medicine,
Umm Al-Qura University, Makkah, KSA
2Department of Oral Biology and Dental Anatomy, Faculty of Dentistry, Al-Azhar University, Egypt
*Corresponding Author: Sherif S Hassan, Department of Basic and Clinical Oral
Sciences, Faculty of Dental Medicine, Umm Al-Qura University, Makkah, KSA.
Received: January 08, 2024; Published: January 22, 2024
Abstract
Objectives: This study aimed to analyse the histopathological and immunohistochemical expression of proliferating cell nuclear antigen (PCNA) and cytokeratin 17 in serous acini of Von Ebner glands of the irradiated versus non irradiated rats for head and neck malignancy to provide a more detailed profile of the radiation injury of the head and neck region.
Methods: Twenty male adult albino rats were divided into two groups; control group received no radiation and irradiated group received a radiation dose of 5 Gy daily for five consecutive days with a total dose of 25 Gy using therapeutic X-ray beam. One month after the last dose of irradiation, rats were euthanized and the tongue was carefully dissected out, fixed, and stained with H&E for routine histopathological examinations. Immunohistochemical staining was performed using antibodies specific for the expression of both proliferating cell nuclear antigen (PCNA) and cytokeratin 17 (CK17).
Results: Histological findings confirmed that the parenchyma of Von Ebner's gland in the radiation-exposed group had glandular atrophy characterized by loss of gland architecture, degenerated acini, and dilatation of the ductal system. Furthermore, there is a predominance of the fibrous component with the presence of fatty degeneration within the glandular tissue. Expression of PCNA in control Von Ebner gland revealed negative to weak reactivity, whereas the irradiated group showed moderate to strong staining in the gland parenchyma. Expression of CK17 in irradiated Von Ebner glands revealed significant moderate to strong reactivity in the acinar and ductal cells compared with weak to mild reactivity in control. The staining expression of irradiated group was varied from diffuse to locally concentrated at the apical cell part.
Conclusion: The severity and prevalence of PCNA and CK17 in the irradiated group from our results suggest a pathological effect that interferes with saliva production and/or secretion leading to xerostomia. Also, the intensity of PCNA expression in that group could be a pathogenic factor in carcinogenesis rather than the healing process in the serous apocrine glands.
Keywords:Radiotherapy; Cytokeratin 17; PCNA; Fractionated; Von Ebner Glan
References
- Alqahtani Mashael Saeed and Sherif Sayed Hassan. “Immunohistochemical Evaluation of the Pathological Effects of Diabetes Mellitus on the Major Salivary Glands of Albino Rats”. European Journal of Dentistry 2 (2023): 485-491.
- Sherif Hassan and Ibraheem Bamaga. “Proliferative Activity of Myoepithelial Cells in Normal and Diabetic Parotid Glands Based on Double Immunostaining Labeling” Open Access Macedonian”. Journal of Medical Sciences 11 (2023) 108-114.
- Dodds, Michael., et al. “Health benefits of saliva: a review”. Journal of Dentistry3 (2005): 223-233.
- Schipper Raymond G., et al. “Saliva as research material: biochemical, physicochemical and practical aspects”. Archives of Oral Biology12 (2007): 1114-1135.
- Avila Jennifer L., et al. “Radiation-induced salivary gland dysfunction results from p53-dependent apoptosis”. International Journal of Radiation Oncology, Biology, Physics2 (2009): 523-529.
- Maria OM., et al. “Effects of double ligation of Stensen's duct on the rabbit parotid gland”. Biotechnic and Histochemistry: Official Publication of the Biological Stain Commission 3 (2014): 181-198.
- Bray Freddie., et al. “Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries”. CA: a Cancer Journal for Clinicians6 (2018): 394-424.
- El-Haddad., et al. “Effects of dose-dependent response to gamma radiation on circumvallate papilla by expression of caspase-3 in vivo”. The Saudi Dental Journal8 (2021): 869-876.
- Vissink A., et al. “Oral sequelae of head and neck radiotherapy”. Critical Reviews in Oral Biology and Medicine: An Official Publication of the American Association of Oral Biologists 3 (2003): 199-212.
- Dorr Wolfgang., et al. “Radiation-induced changes in cellularity and proliferation in human oral mucosa”. International Journal of Radiation Oncology, Biology, Physics4 (2002): 911-917.
- Bazyka D., et al. “Buccal mucosa micronuclei counts in relation to exposure to low dose-rate radiation from the Chornobyl nuclear accident and other medical and occupational radiation exposures”. Environmental Health: A Global Access Science Source1 (2017): 70.
- Hassan Sherif., et al. “Distribution of Cytokeratin 17 in the Parenchymal Elements of Rat's Submandibular Glands Subjected to Fractionated Radiotherapy”. European Journal of Dentistry 3 (2020): 440-447.
- Hassan Sherif Sayed and Mashael Saeed Alqahtani. “Comparative Study of Cytokeratin Immunostaining of Parotid Gland Parenchyma in Normal, Diabetic, and Excretory Duct Ligation of Mongrel Dogs”. European Journal of Dentistry 3 (2023): 678-686.
- Bravo R and H Macdonald-Bravo. “Existence of two populations of cyclin/proliferating cell nuclear antigen during the cell cycle: association with DNA replication sites”. The Journal of Cell Biology 4 (1987): 1549-1554.
- Burgess KL., et al. “Myoepithelial cells actively proliferate during atrophy of rat parotid gland”. Oral Surgery, Oral Medicine, Oral pathology, Oral Radiology, and Endodontics6 (1996): 674-680.
- Elabasiry Magdy., et al. “Expression of cytokeratin 17 in normal and diabetic submandibular salivary gland (histological and immunohistochemical study)”. Tanta Dental Journal4 (2018): 241-246.
- Jasmer Kimberly J., et al. “Radiation-Induced Salivary Gland Dysfunction: Mechanisms, Therapeutics and Future Directions”. Journal of Clinical Medicine12 (2020): 4095.
- Niedermeier W., et al. “Radiation-induced hyposalivation and its treatment with oral pilocarpine”. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics5 (1998): 541-549.
- Boraks George., et al. “Effect of ionizing radiation on rat parotid gland”. Brazilian Dental Journal1 (2008): 73-76.
- Limesand Kirsten H., et al. “Suppression of radiation-induced salivary gland dysfunction by IGF-1”. PloS one3 (2009): e4663.
- Grundmann O., et al. “Sensitivity of salivary glands to radiation: from animal models to therapies”. Journal of Dental Research10 (2009): 894-903.
- Paardekooper GM., et al. “Radiation-induced apoptosis in relation to acute impairment of rat salivary gland function”. International Journal of Radiation Biology6 (1998): 641-648.
- Marmary Yitzhak., et al. “Radiation-Induced Loss of Salivary Gland Function Is Driven by Cellular Senescence and Prevented by IL6 Modulation”. Cancer Research5 (2016): 1170-1180.
- Modan B., et al. “Increased risk of salivary gland tumors after low-dose irradiation”. The Laryngoscope7 (1998): 1095-1097.
- Spraggs PD., et al. “post-irradiation carcinosarcoma of the parotid gland”. The Journal of Laryngology and Otology5 (1994): 443-445.
- Peter B., et al. “Radiation-induced cell proliferation in the parotid and submandibular glands of the rat”. Radiation Research2 (1994): 257-265.
- Haghighat N and I Al-Hashimi. “A pilot study on the effect of radiation on calmodulin in rat submandibular salivary glands”. Archives of Oral Biology5 (1999): 383-389.
- Coppes RP., et al. “Early radiation effects on muscarinic receptor-induced secretory responsiveness of the parotid gland in the freely moving rat”. Radiation Research3 (2000): 339-346.
- Bartel-Friedrich., et al. “Immunohistochemical detection of cytokeratins in the irradiated rat mandibular gland”. Anticancer Research4A (1999): 2405-2409.
- Bartel-Friedrich., et al. “Dose-response relationships on the expression profile of cytokeratins and vimentin in rat submandibular glands following fractionated irradiation”. Anticancer Research6D (2000): 4917-4926.
- Gustafsson H., et al. “Effects of fractionated irradiation on the cytoskeleton and basal lamina in parotid glands--an immunohistochemical study”. Acta Oncologica (Stockholm, Sweden) 1 (1998): 33-40.
- Bonan Paulo Rogério Ferreti., et al. “Cytokeratin expression in initial oral mucositis of head and neck irradiated patients”. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics2 (2006): 205-211.
Citation
Copyright