Literature DB >> 16109353

Cell-mediated immunity and head and neck cancer: with special emphasis on betel quid chewing habit.

M C Chang1, C P Chiang, C L Lin, J J Lee, L J Hahn, J H Jeng.   

Abstract

Betel quid (BQ) chewing is popular in Taiwan, India, and many southeast-Asian countries. BQ chewing has strong association with the risk of oral leukoplakia (OL), oral submucous fibrosis (OSF), and oral cancer (OC). BQ components exhibit genotoxicity and may alter the structure of DNA, proteins and lipids, resulting in production of antigenicity. BQ ingredients are also shown to induce keratinocyte inflammation by stimulating the production of prostaglandins, TNF-alpha, IL-6, IL-8, and granulocyte-macrophage colony-stimulating factor (GM-CSF) in keratinocytes. These events may provoke tissue inflammation, early cell-mediated immunity (CMI), and immune surveillance in BQ chewers. However, BQ components also directly affect the functional activities of immunocompotent cells, and moreover tumor cells may hypo-respond to the CMI via diverse mechanisms such as induction of apoptosis of lymphocytes, induction of production of suppressor T cells, downregulation of MHC molecules in tumor cells, etc. Clinically, an alteration in lymphocyte subsets, a decrease in total number of lymphocytes, and a reduction in functional activities of CMI have been observed in isolated peripheral blood mononuclear cells (PBMC) and tumor infiltrated lymphocytes (TIL) in patients with OSF, OL or OC. Adaptation of tumor cells to immune system may promote clonal selection of resistant tumor cells, leading to immune tolerance. Future studies on effects of BQ components on CMI and humoral immunity in vitro and in vivo can be helpful for chemoprevention of BQ-related oral mucosal diseases. To elucidate how virus infection, tobacco, alcohol and BQ consumption, and other environmental exposure affect the immune status of patients with oral premalignant lesions or OC will help us to understand the immunopathogenesis of OC and to develop immunotherapeutic strategies for OC.

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Mesh:

Year:  2005        PMID: 16109353     DOI: 10.1016/j.oraloncology.2005.01.007

Source DB:  PubMed          Journal:  Oral Oncol        ISSN: 1368-8375            Impact factor:   5.337


  20 in total

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3.  Role of inflammation in oral carcinogenesis (Part I): Histological grading of malignancy using a binary system.

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4.  Skewed immunological balance between Th17 (CD4(+)IL17A (+)) and Treg (CD4 (+)CD25 (+)FOXP3 (+)) cells in human oral squamous cell carcinoma.

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6.  Characterization of the psychological, physiological and EEG profile of acute betel quid intoxication in naïve subjects.

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Journal:  PLoS One       Date:  2011-08-31       Impact factor: 3.240

7.  Correlates of anti-EBV EBNA1 IgA positivity among unaffected relatives from nasopharyngeal carcinoma multiplex families.

Authors:  C M Chang; K J Yu; W L Hsu; J M Major; J Y Chen; P J Lou; M Y Liu; S R Diehl; A M Goldstein; C J Chen; A Hildesheim
Journal:  Br J Cancer       Date:  2011-11-17       Impact factor: 7.640

8.  Cytomorphometric analysis of squames obtained from normal mucosa, leukoplakia and oral squamous cell carcinoma.

Authors:  T Suresh; T Sabastian Bastian; B R Ahmed Mujib
Journal:  J Oral Maxillofac Pathol       Date:  2021-05-14

9.  Immunohistochemical evaluation of mast cells and vascular endothelial proliferation in oral precancerous lesion-leukoplakia.

Authors:  M Sathyakumar; G Sriram; Tr Saraswathi; B Sivapathasundharam
Journal:  J Oral Maxillofac Pathol       Date:  2012-09

10.  Oral and pharyngeal cancer in South Asians and non-South Asians in relation to socioeconomic deprivation in South East England.

Authors:  D R Moles; S Fedele; P M Speight; S R Porter; I dos Santos Silva
Journal:  Br J Cancer       Date:  2008-01-22       Impact factor: 7.640

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