Academic literature on the topic 'Colon (Anatomy) Cancer Genetic aspects'

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Journal articles on the topic "Colon (Anatomy) Cancer Genetic aspects"

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Martianov, Aleksandr S., Ekaterina Sh Kuligina, Alexandr A. Romanko, and Evgeny N. Imyanitov. "Molecular genetic testing in colon cancer: clinical aspects." Almanac of Clinical Medicine 50, no. 1 (2022): 1–12. http://dx.doi.org/10.18786/2072-0505-2022-50-002.

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Molecular genetic diagnostics is an essential element to plan for management of colorectal cancer (CRC) patients. The choice of systemic treatment for CRC is impossible without molecular testing of the tumor. For instance, the assessment of the KRAS and NRAS genes is mandatory for consideration of anti-EGFR agents. Tumors with BRAF V600E mutation are characterized by aggressive behavior, the necessity of intensive cytostatic regimens, as well as by sensitivity to combination therapy with BRAF and EGFR inhibitors. Inactivation of the DNA mismatch repair, the MUTYH gene or DNA polymerase epsilon
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Lynch, Patrick M. "Medicolegal Aspects of Endoscopic Screening and Genetic Testing in Hereditary Colon Cancer Syndromes." Techniques in Gastrointestinal Endoscopy 8, no. 3 (2006): 133–39. http://dx.doi.org/10.1016/j.tgie.2006.04.004.

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Semyanikhina, A. V., A. O. Rasulov, and L. N. Lyubchenko. "Clinical and genetic aspects of differential diagnostics of hereditary non-polyposis colorectal cancer." Advances in molecular oncology 6, no. 2 (2019): 21–27. http://dx.doi.org/10.17650/2313-805x-2019-6-2-21-27.

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Lynch syndrome was synonymous with hereditary non-polyposis colorectal cancer for a long time, however, mapping of the DNA mismatch repair (MMR) genes has led to distinguish Lynch syndrome as an independent syndromic unit from a number of Lynch-like syndromes that phenotypically mimic with the most frequent hereditary variant of colon cancer but genetically representing quite a heterogeneous group. This article presents up to date clinical and genetic characteristics of Lynch syndrome and Lynch-like conditions.
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Augestad, Knut Magne, Marianne A. Merok, and Dejan Ignatovic. "Tailored Treatment of Colorectal Cancer: Surgical, Molecular, and Genetic Considerations." Clinical Medicine Insights: Oncology 11 (January 1, 2017): 117955491769076. http://dx.doi.org/10.1177/1179554917690766.

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Colorectal cancer (CRC) is a complex cancer disease, and approximately 40% of the surgically cured patients will experience cancer recurrence within 5 years. During recent years, research has shown that CRC treatment should be tailored to the individual patient due to the wide variety of risk factors, genetic factors, and surgical complexity. In this review, we provide an overview of the considerations that are needed to provide an individualized, patient-tailored treatment. We emphasize the need to assess the predictors of CRC, and we summarize the latest research on CRC genetics and immunoth
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Hoffmann, Diane E., and Eric A. Wulfsberg. "Testing Children for Genetic Predispositions: Is it in Their Best Interest?" Journal of Law, Medicine & Ethics 23, no. 4 (1995): 331–44. http://dx.doi.org/10.1111/j.1748-720x.1995.tb01375.x.

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Researchers summoned a Baltimore County woman to an office at the Johns Hopkins School of Public Health last spring to tell her the bad news. They had found a genetic threat lurking in her 7-year-old son's DNA—a mutant gene that almost always triggers a rare form of colon cancer. It was the same illness that led surgeons to remove her colon in 1979. While the boy, Michael, now 8, is still perfectly healthy, without surgery he is almost certain to develop cancer by age 40.This genetic fortune-telling was no parlor trick. It was the product of astonishing advances in recent decades in understand
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Yaméogo, P. B., R. A. Djigemde, M. Ilboudo, A. S. Ouedraogo, and N. Zongo. "Descriptive epidemiology of colorectal cancer in Burkina Faso." African Journal of Oncology 2, no. 2 (2022): 54–57. http://dx.doi.org/10.54266/ajo.2.2.54.

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OBJECTIVE: To describe the epidemiological profile of colorectal cancers in Burkina Faso. MATERIALS AND METHODS: This was a cross-sectional and descriptive study of colorectal cancers diagnosed in all anatomy and pathology laboratories in Burkina Faso from 1988 to 2018. Age, sex, nature of the specimens, histo-genetic and histological types were studied. Comparisons were possible using Student's t test and Fisher's Khi2 test. RESULTS: In 31 years, 802 colorectal cancers were diagnosed, representing a mean annual incidence of 25.9 cases ± 7.6. These cancers represented 30.9% of all digestive ca
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Ehrenfeld, Maximilian, Anna Schrade, Tatiana Flisikowska, et al. "Tumor Targeting with Bacterial Shiga Toxin B Subunit in Genetic Porcine Models for Colorectal Cancer and Osteosarcoma." Molecular Cancer Therapeutics 21, no. 4 (2022): 686–99. http://dx.doi.org/10.1158/1535-7163.mct-21-0445.

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Abstract The B subunit of bacterial Shiga toxin (STxB) is nontoxic and has low immunogenicity. Its receptor, the glycosphingolipid Gb3/CD77, is overexpressed on the cell surface of human colorectal cancer. We tested whether genetic porcine models, closely resembling human anatomy and pathophysiology, can be used to exploit the tumor-targeting potential of STxB. In accordance with findings on human colorectal cancer, the pig model APC1311 bound STxB in colorectal tumors, but not in normal colon or jejunum, except for putative enteroendocrine cells. In primary tumor cells from endoscopic biopsie
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Pancione, Massimo, Andrea Remo, and Vittorio Colantuoni. "Genetic and Epigenetic Events Generate Multiple Pathways in Colorectal Cancer Progression." Pathology Research International 2012 (July 24, 2012): 1–11. http://dx.doi.org/10.1155/2012/509348.

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Colorectal cancer (CRC) is one of the most common causes of death, despite decades of research. Initially considered as a disease due to genetic mutations, it is now viewed as a complex malignancy because of the involvement of epigenetic abnormalities. A functional equivalence between genetic and epigenetic mechanisms has been suggested in CRC initiation and progression. A hallmark of CRC is its pathogenetic heterogeneity attained through at least three distinct pathways: a traditional (adenoma-carcinoma sequence), an alternative, and more recently the so-called serrated pathway. While the alt
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Aceto, Gitana Maria, Teresa Catalano, and Maria Cristina Curia. "Molecular Aspects of Colorectal Adenomas: The Interplay among Microenvironment, Oxidative Stress, and Predisposition." BioMed Research International 2020 (March 16, 2020): 1–19. http://dx.doi.org/10.1155/2020/1726309.

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The development of colorectal cancer (CRC) is a multistep process initiated by a benign polyp that has the potential to evolve into in situ carcinoma through the interactions between environmental and genetic factors. CRC incidence rates are constantly increased for young adult patients presenting an advanced tumor stage. The majority of CRCs arise from colonic adenomas originating from aberrant cell proliferation of colon epithelium. Endoscopic polypectomy represents a tool for early detection and removal of polyps, although the occurrence of cancers after negative colonoscopy shows a signifi
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Djadou, Teresa Moreno, Antonio Rey, Javier Die, Eduardo Lobo, and Juan Carlos García Pérez. "Colorectal Cancer: Comparative Analysis Between Two Series of Patients Separated by More Than Three Decades." Journal of Coloproctology 42, no. 03 (2022): 266–72. http://dx.doi.org/10.1055/s-0042-1755240.

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Abstract Aim This study characterizes Colorectal Cancer (CRC) incidence in the University Hospital Ramon and Cajal, Madrid, and analyzes variations over time. It establishes risk groups, aiming to discover whether diagnosis can be determined in less advanced stages of disease. Method Evolutionary epidemiological study of genetic and environmental factors contributing to the development of CRC in this district that enables the comparison of two cohorts of patients separated by 37 years: G1 (patients of current group) and G2 (patients of historical group). The main risk variables gleaned retrosp
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Dissertations / Theses on the topic "Colon (Anatomy) Cancer Genetic aspects"

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Butler, Lisa Maree. "Molecular analysis of the human Fas gene in colorectal cancer /." Title page, contents and summary only, 1998. http://web4.library.adelaide.edu.au/theses/09PH/09phb9858.pdf.

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陳安安 and On-on Annie Chan. "Methylation in colorectal cancer." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2002. http://hub.hku.hk/bib/B25256312.

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Warusavitarne, Janindra. "Analysis of the factors that influence the biological behaviour and response to chemotherapy in sporadic colorectal carcinomas with microsatellite instability." Thesis, The University of Sydney, 2005. https://hdl.handle.net/2123/27920.

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High frequency microsatellite instability (MSI—H) is an alternate pathway of colorectal carcinogenesis and is present in approximately 15% of all sporadic colorectal cancers. These tumours are predominantly located in the right colon, occur mainly in the elderly and have a better prognosis than microsatellite stable (MSS) CRCs. In addition they are usually of mucinous type histology, tend to be locally invasive, metastasise less and are of larger size than MSS CRCs. The mismatch repair (MMR) genes hMLHl is most commonly mutated or methylated in sporadic colorectal cancers with MSI-H.
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Li, Carmen, and 李嘉敏. "Characterisation of methylator phenotype of colorectal cancer in young patients." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hdl.handle.net/10722/207182.

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The majority of sporadic colorectal cancer (CRC) cases affects individuals over the age of 50, but about 10% of cases occur in young adults under 50 in Hong Kong. Apart from germline mutation of the DNA mismatch repair genes that predisposes to early-onset CRC with a high-level of microsatellite instability (MSI-H), it is unknown if the mechanisms that give rise to CRC in other young adults differ from those in older individuals. In an effort to understand the genetic and epigenetic basis of early and late-onset CRC outside the Lynch Syndrome setting, we performed a detailed characterization o
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Mui, Kin-cheong, and 梅堅祥. "Inactivation of DNA match repair proteins in premalignant lesions in Lynch syndrome." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B44659635.

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Tai, Bik-wah Diana, and 戴碧華. "Haplotype analysis of the family with Lynch syndrome." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B45153772.

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Wright, C. M. "The prognostic significance of microsatellite instability in sporadic stage C colorectal cancer." Thesis, The University of Sydney, 2008. https://hdl.handle.net/2123/28955.

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Identification and understanding of the molecular events involved in colorectal cancer (CRC) pathogenesis should lead to better comprehension of the disease process, hopefully leading to better prognostic stratification, and as a result more targeted treatment regimens and improved patient outcomes. A sub group of sporadic CRC exhibit microsatellite instability (MSI). MSI is seen when the fidelity of DNA replication is impaired. Cancers may be categorized as MSI-high (MSI-H), MSI-low (MSI-L), or microsatellite stable (MSS), according to the degree of MSI exhibited. This research proj
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Siu, Ho-yee Vivian. "The role of monitoring style in managing psychological distress associated with genetic colorectal cancer testing." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B29760161.

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陳俊良 and Tsun-leung Chan. "Genomic instability and DNA mismatch repair gene mutations in colorectal cancer." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1999. http://hub.hku.hk/bib/B31238221.

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Chan, Ling-fung, and 陳凌鋒. "Expression of the DNA mismatch repair protein MLH1 in serrated polyps of the colon: an immunohistochemical study." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2005. http://hub.hku.hk/bib/B45010584.

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Books on the topic "Colon (Anatomy) Cancer Genetic aspects"

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M, Lynch Patrick, and Lynch Henry T, eds. Colon cancer genetics. Van Nostrand Reinhold Co., 1985.

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Genetics of colorectal cancer for clinical practice. Kluwer Academic Publishers, 1993.

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Höwer, Sybille. Gesundheitsverhalten bei vererbbarem Darmkrebs HNPCC (hereditary non-polyposis colorectal cancer): Unter besonderer Berücksichtigung von Kontroll- und Kompetenüberzeugungen : eine sozialpsychologische Studie im Rahmen des von der Deutschen Krebshilfe geförderten Forschungsprojekts "Familiärer Darmkrebs". Peter Lang, 2005.

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Kjetil, Søreide, and Søiland Håvard, eds. Clinical, genetic, and molecular precursor features in colorectal neoplasia. Nova Science, 2008.

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G, Williams Bryan R., and Casey Graham, eds. Molecular genetics and colorectal neoplasia: A primer for the clinician. Igaku-Shoin, 1996.

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Parker, James N., and Philip M. Parker. Hereditary nonpolyposis colorectal cancer: A bibliography and dictionary for physicians, patients, and genome researchers [to internet references]. ICON Health Publications, 2007.

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Parker, James N., and Philip M. Parker. Familial adenomatous polyposis: A bibliography and dictionary for physicians, patients, and genome researchers [to internet references]. ICON Health Publications, 2007.

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International Symposium on Colorectal Cancer (4th 1989 Kōbe-shi, Japan). Hereditary colorectal cancer: Proceedings of the fourth International Symposium on Colorectal Cancer (ISCC-4), November 9-11, 1989, Kobe, Japan. Springer-Verlag, 1990.

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Turk, Emily R. Digest of innovative strategies in colorectal cancer prevention. Cancer Research and Prevention Foundation, 2004.

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1926-, Lipkin Martin, Newmark Harold L, Kelloff Gary, and National Cancer Institute (U.S.). Chemoprevention Branch., eds. Calcium, vitamin D, and prevention of colon cancer. CRC Press, 1991.

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Book chapters on the topic "Colon (Anatomy) Cancer Genetic aspects"

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"Chemical Carcinogenesis and Mutagenesis." In Environmental Toxicology, edited by Sigmund F. Zakrzewski. Oxford University Press, 2002. http://dx.doi.org/10.1093/oso/9780195148114.003.0010.

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Cancer is a common name for about 200 diseases characterized by abnormal cell growth. According to Kundson (1), the causes of cancer may be classified into the following groups: 1. genetic predisposition 2. environmental factors 3. environmental factors superimposed on genetic predisposition 4. unknown factors Typical examples of the first group are childhood cancers such as retinoblastoma (a genetically predisposed malignancy of the retina), neuroblastoma (a malignancy of the brain), and Wilms’ tumor (a malignancy of the kidney). In adults, an example is polyposis of the colon, a genetic condition that frequently leads to colon cancer. The third group is represented by xeroderma pigmentosum, a genetic condition characterized by a deficient DNA excision repair mechanism (see the discussion later in this chapter). Individuals so predisposed develop skin cancer when exposed to ultraviolet light. The variable susceptibility of the population to the carcinogenic effects of cigarette smoke may also reflect genetic predisposition. Very little can be said about the fourth group because the causes of this group of cancers are not known. Groups 2 and 3 combined (i.e., cancer attributable to environmental causes, with or without genetic predisposition) probably account for 60– 90% of all cancers (2). The environment, in this context, involves not only air, water, and soil, but also food, drink, living habits, occupational exposure, drugs, and practically all aspects of human interaction with the surroundings. This definition implies that a great majority of cancers could be prevented by avoiding exposure to potential carcinogens and by changing living habits. It is therefore not surprising that the study of chemical carcinogenesis represents a major aspect of environmental toxicology. Table 5.1 gives an overview of estimated environmentally associated cancer mortality or incidence in the United States. The data presented in this table have to be considered as rough estimates only. There are great variations in the estimates, depending on the investigators and their methods of collecting the pertinent statistics. The Office of Technology Assessment report on cancer risk offers a more in-depth treatment of this subject.
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