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      Orabase-Formulated Benzalkonium Chloride Effectively Suppressed Oral Potentially Malignant Disorder In Vitro and In Vivo

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          Abstract

          Oral potentially malignant disorder (OPMD) is associated with an increased risk of progression to oral cancer. Patients with dysplastic changes of the precancerous lesions have a higher malignant transformation rate than those without dysplastic changes. Radiotherapy and surgery are the traditionally preferred choices for OPMD treatment. However, side effects caused by radiotherapy and surgery may reduce the willingness of patients to accept therapy. Therefore, developing an Orabase-formulated drug, which can be non-invasively administered, may provide an alternative treatment choice. To find, verify, and develop a new anti-cancer drug cost a lot of time and money, while drug repurposing can shorten both time and cost. In this study, we utilized high-throughput screening library to identify clinical drugs, which may have new bioactivities. Herein, we report that benzalkonium chloride (BAK), an antimicrobial preservative for pharmaceutical products, significantly induced reactive oxygen species production and cell death in oral precancerous cells. Additionally, our results showed that phosphorylation of STAT3 (Tyr705) and Akt (Ser473) were involved in cell death caused by BAK in DOK cells. According to animal studies, the development of DMBA-induced oral precancerous lesions was inhibited by 2% BAK. In conclusion, Orabase-formulated BAK may be a potential treatment for OPMD in the future.

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          Most cited references21

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          Regulation of p53 in response to DNA damage.

          Activation of p53 can occur in response to a number of cellular stresses, including DNA damage, hypoxia and nucleotide deprivation. Several forms of DNA damage have been shown to activate p53, including those generated by ionising radiation (IR), radio-mimetic drugs, ultraviolet light (UV) and chemicals such as methyl methane sulfonate (MMS). Under normal conditions, p53 levels are maintained at a low state by virtue of the extremely short-half life of the polypeptide. In addition to this, p53 normally exists in an largely inactive state that is relatively inefficient at binding to DNA and activating transcription. Activation of p53 in response to DNA damage is associated with a rapid increase in its levels and with an increased ability of p53 to bind DNA and mediate transcriptional activation. This then leads to the activation of a number of genes whose products trigger cell-cycle arrest, apoptosis, or DNA repair. Recent work has suggested that this regulation is brought about largely through DNA damage triggering a series of phosphorylation, de-phosphorylation and acetylation events on the p53 polypeptide. Here, we discuss the nature of these modifications, the enzymes that bring them about, and how changes in p53 modification lead to p53 activation.
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            Benzalkonium Chlorides: Uses, Regulatory Status, and Microbial Resistance

            Benzalkonium chlorides (BACs) are chemicals with widespread applications due to their broad-spectrum antimicrobial properties against bacteria, fungi, and viruses. This review provides an overview of the market for BACs, as well as regulatory measures and available data on safety, toxicity, and environmental contamination. We focus on the effect of frequent exposure of microbial communities to BACs and the potential for cross-resistant phenotypes to emerge. Toward this goal, we review BAC concentrations in consumer products, their correlation with the emergence of tolerance in microbial populations, and the associated risk potential. Our analysis suggests that the ubiquitous and frequent use of BACs in commercial products can generate selective environments that favor microbial phenotypes potentially cross-resistant to a variety of compounds. An analysis of benefits versus risks should be the guidepost for regulatory actions regarding compounds such as BACs.
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              Is Open Access

              Histological and molecular aspects of oral squamous cell carcinoma (Review)

              Oral squamous cell carcinoma (OSCC) represents 95% of all forms of head and neck cancer, and over the last decade its incidence has increased by 50%. Oral carcinogenesis is a multistage process, which simultaneously involves precancerous lesions, invasion and metastasis. Degradation of the cell cycle and the proliferation of malignant cells results in the loss of control mechanisms that ensure the normal function of tissues. The aim of the current review is to present the histopathological features of OSCC, including potentially malignant changes, the international classification of tumors, the tumor invasion front and tumor biomarkers (Ki-67, p53, homeobox genes and collagen type IV), as well as the tumor microenvironment and function of cancer-associated fibroblasts in the most common type of oral cancer that is encountered by dental surgeons. In OSCC, associations have been identified between the proliferation, basal lamina degradation and connective tissue modulation. Therefore, the comparison of these factors with the survival time of OSCC patients from the histopathological diagnosis is of interest.
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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                23 March 2020
                31 March 2020
                : 5
                : 12
                : 7018-7024
                Affiliations
                []School of Dentistry, College of Dental Medicine, Kaohsiung Medical University , Kaohsiung, Taiwan
                []Center for Cancer Research, Kaohsiung Medical University , Kaohsiung, Taiwan
                [§ ]Department of Medical Research, Kaohsiung Medical University Hospital, Kaohsiung Medical University , Kaohsiung 807, Taiwan
                []Division of Oral Pathology&Maxillofacial Radiology, Kaohsiung Medical University Hospital , Kaohsiung 807, Taiwan
                []Oral & Maxillofacial Imaging Center, College of Dental Medicine, Kaohsiung Medical University , Kaohsiung 807, Taiwan
                [# ]School of Pharmacy, Kaohsiung Medical University , Kaohsiung 807, Taiwan
                []Department of Dermatology, College of Medicine, Kaohsiung Medical University , Kaohsiung 807, Taiwan
                []Department of Dermatology, Kaohsiung Medical University Hospital, Kaohsiung Medical University , Kaohsiung 807, Taiwan
                []Translational Research Center, Kaohsiung Medical University Hospital, Kaohsiung Medical University , Kaohsiung 807, Taiwan
                []Department of Obstetrics and Gynecology, Kaohsiung Medical University Hospital, Kaohsiung Medical University , Kaohsiung 807, Taiwan
                [& ]Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University , Kaohsiung 807, Taiwan
                Author notes
                [* ]Email: yuanssf@ 123456ms33.hinet.net . Tel. No.: +886-7-3121101#2557.
                Article
                10.1021/acsomega.0c00640
                7114696
                1e5e22b6-fce9-4c97-91e5-b65142935e38
                Copyright © 2020 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 12 February 2020
                : 12 March 2020
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