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      Expression of p53, p63, podoplanin and Ki-67 in recurring versus non-recurring oral leukoplakia

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          Abstract

          Oral leukoplakia (OL), a potentially malignant disorder, recurs in 40% of cases after surgical removal. Recurrence is a risk factor for malignant transformation. We aimed to examine the prognostic significance of four biomarkers related to cell proliferation: p53, p63, podoplanin (PDPN) and Ki-67 in predicting recurrence. Formalin-fixed-paraffin-embedded specimens from excised OL (n = 73, 33 recurrent; 40 non-recurrent) were collected in a prospective study. Immunohistochemistry was used to visualise expression of p53, p63, PDPN and Ki-67. Image analysis software was used for quantification of p53-, p63- and Ki-67-expressing cells, while PDPN was analysed visually. The expression of all four proteins were higher in recurrent compared with non-recurrent OL, only expression of p53 was statistically significant. In uni- and multivariable Cox regression analyses of individual markers, expression of p63 was significantly associated with higher recurrence risk ( p = 0.047). OL with a combined high expression of both p53 and p63 had a significantly higher risk to recur [Log Rank, p = 0.036; multivariate Cox, HR: 2.48 (1.13–5.44; p = 0.024)]. Combination of p53 and p63 expression may be used as a prognostic biomarker for recurrence of OL.

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          Most cited references43

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          Hallmarks of Cancer: The Next Generation

          The hallmarks of cancer comprise six biological capabilities acquired during the multistep development of human tumors. The hallmarks constitute an organizing principle for rationalizing the complexities of neoplastic disease. They include sustaining proliferative signaling, evading growth suppressors, resisting cell death, enabling replicative immortality, inducing angiogenesis, and activating invasion and metastasis. Underlying these hallmarks are genome instability, which generates the genetic diversity that expedites their acquisition, and inflammation, which fosters multiple hallmark functions. Conceptual progress in the last decade has added two emerging hallmarks of potential generality to this list-reprogramming of energy metabolism and evading immune destruction. In addition to cancer cells, tumors exhibit another dimension of complexity: they contain a repertoire of recruited, ostensibly normal cells that contribute to the acquisition of hallmark traits by creating the "tumor microenvironment." Recognition of the widespread applicability of these concepts will increasingly affect the development of new means to treat human cancer. Copyright © 2011 Elsevier Inc. All rights reserved.
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            QuPath: Open source software for digital pathology image analysis

            QuPath is new bioimage analysis software designed to meet the growing need for a user-friendly, extensible, open-source solution for digital pathology and whole slide image analysis. In addition to offering a comprehensive panel of tumor identification and high-throughput biomarker evaluation tools, QuPath provides researchers with powerful batch-processing and scripting functionality, and an extensible platform with which to develop and share new algorithms to analyze complex tissue images. Furthermore, QuPath’s flexible design makes it suitable for a wide range of additional image analysis applications across biomedical research.
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              Mutant p53: one name, many proteins.

              There is now strong evidence that mutation not only abrogates p53 tumor-suppressive functions, but in some instances can also endow mutant proteins with novel activities. Such neomorphic p53 proteins are capable of dramatically altering tumor cell behavior, primarily through their interactions with other cellular proteins and regulation of cancer cell transcriptional programs. Different missense mutations in p53 may confer unique activities and thereby offer insight into the mutagenic events that drive tumor progression. Here we review mechanisms by which mutant p53 exerts its cellular effects, with a particular focus on the burgeoning mutant p53 transcriptome, and discuss the biological and clinical consequences of mutant p53 gain of function.
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                Author and article information

                Contributors
                bengt.hasseus@gu.se
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                21 October 2021
                21 October 2021
                2021
                : 11
                : 20781
                Affiliations
                [1 ]GRID grid.8761.8, ISNI 0000 0000 9919 9582, Department of Oral Medicine and Pathology, Institute of Odontology, The Sahlgrenska Academy, , University of Gothenburg, ; P.O. Box 450, 40530 Gothenburg, Sweden
                [2 ]GRID grid.5510.1, ISNI 0000 0004 1936 8921, Department of Oral Biology, , University of Oslo, ; Oslo, Norway
                [3 ]GRID grid.8761.8, ISNI 0000 0000 9919 9582, Department of Oncology, Institute of Clinical Sciences, The Sahlgrenska Academy, , University of Gothenburg, ; Gothenburg, Sweden
                [4 ]GRID grid.8761.8, ISNI 0000 0000 9919 9582, Department of Oral and Maxillofacial Surgery, Institute of Odontology, The Sahlgrenska Academy, , University of Gothenburg, ; Gothenburg, Sweden
                [5 ]GRID grid.1649.a, ISNI 000000009445082X, Department of Clinical Pathology, , Sahlgrenska University Hospital, ; Gothenburg, Sweden
                [6 ]GRID grid.25769.3f, ISNI 0000 0001 2169 7132, Department of Oral Pathology, Faculty of Dentistry, , Gazi University, ; Ankara, Turkey
                [7 ]Clinic of Oral Medicine, Public Dental Service, Region Västra Götaland, Gothenburg, Sweden
                Article
                99326
                10.1038/s41598-021-99326-5
                8531318
                34675318
                6558b87e-e1b1-4425-b5c2-0384f3ea6c4c
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 20 April 2021
                : 6 September 2021
                Funding
                Funded by: The Healthcare Board, Region Västra Götaland (Hälso- och sjukvårdsstyrelsen), TUA Research
                Funded by: The Sahlgrenska Academy at the University of Gothenburg/Region Västra Götaland, Assar Gabrielsson Foundation, Adlerbertska Foundation
                Funded by: Swedish Dental Society
                Funded by: Gothenburg Dental Society
                Funded by: Tannlegevitenskapens fremme for DS, University of Oslo, Norway
                Funded by: University of Gothenburg
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                oral cancer,oral cancer detection
                Uncategorized
                oral cancer, oral cancer detection

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