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Clinical and Developmental Immunology
Volume 2010 (2010), Article ID 170432, 13 pages
Current Hypotheses on How Microsatellite Instability Leads to Enhanced Survival of Lynch Syndrome Patients
1Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, NE 68178, USA
2Department of Pathology, Creighton University School of Medicine, Omaha, NE 68178, USA
3Department of Preventative Medicine, Creighton University School of Medicine, Omaha, NE 68178, USA
Received 8 January 2010; Accepted 13 April 2010
Academic Editor: C. Pauza
Copyright © 2010 Kristen M. Drescher et al. is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Citations to this Article [26 citations]
The following is the list of published articles that have cited the current article.
- Yvette Garbe, Ulrike Klier, and Michael Linnebacher, “Semiallogenic fusions of MSI+ tumor cells and activated B cells induce MSI-specific T cell responses,” Bmc Cancer, vol. 11, 2011.
- Sarah Popek, and Vassiliki L. Tsikitis, “Epidemiology of Inherited Colon Cancer,” Seminars in Colon and Rectal Surgery, vol. 22, no. 2, pp. 77–81, 2011.
- Kimberly D. Siegmund, Paul Marjoram, Simon Tavare, and Darryl Shibata, “High DNA Methylation Pattern Intratumoral Diversity Implies Weak Selection in Many Human Colorectal Cancers,” Plos One, vol. 6, no. 6, 2011.
- Frank A. Sinicrope, and Zhineng Jayson Yang, “Prognostic and predictive impact of DNA mismatch repair in the management of colorectal cancer,” Future Oncology, vol. 7, no. 3, pp. 467–474, 2011.
- Yvette Garbe, Claudia Maletzki, and Michael Linnebacher, “An MSI Tumor Specific Frameshift Mutation in a Coding Microsatellite of MSH3 Encodes for HLA-A0201-Restricted CD8(+) Cytotoxic T Cell Epitopes,” Plos One, vol. 6, no. 11, 2011.
- Cristina Bozzao, Alessandro Stella, and Patrizia Lastella, “Anticipation in Lynch Syndrome: Where We Are Where We Go,” Current Genomics, vol. 12, no. 7, pp. 451–465, 2011.
- Sha-Sha Guan, and Guang-Hai Dai, “Molecular biology and clinical features of hereditary non-polyposis colorectal cancer,” Acta Academiae Medicinae Sinicae, vol. 34, no. 3, pp. 293–297, 2012.
- Noel F. C. C. de Miranda, Danny Goudkade, Ekaterina S. Jordanova, Carli M. J. Tops, Frederik J. Hes, Hans F. A. Vasen, Tom van Wezel, and Hans Morreau, “Infiltration of Lynch Colorectal Cancers by Activated Immune Cells Associates with Early Staging of the Primary Tumor and Absence of Lymph Node Metastases,” Clinical Cancer Research, vol. 18, no. 5, pp. 1237–1245, 2012.
- D. Schiff, E. M. Lam, J. E. Parisi, C. Giannini, J. H. Uhm, B. M. Keegan, and O. H. Kantarci, “A 21-year-old woman with multiple cancers and a new brain lesion,” Neurology, vol. 78, no. 10, pp. 743–749, 2012.
- Jinru Shia, Hangjun Wang, Garrett M. Nash, and David S. Klimstra, “Lymph Node Staging in Colorectal Cancer: Revisiting the Benchmark of at Least 12 Lymph Nodes in R0 Resection,” Journal Of The American College Of Surgeons, vol. 214, no. 3, pp. 348–355, 2012.
- Jeong M. Bae, Nam-Yun Cho, Tae-You Kim, and Gyeong H. Kang, “Clinicopathologic and Molecular Characteristics of Synchronous Colorectal Cancers,” Diseases of the Colon & Rectum, vol. 55, no. 2, pp. 181–190, 2012.
- Amanda I. Phipps, John D. Potter, Polly A. Newcomb, Daniel D. Buchanan, Karen W. Makar, Andrea N. Burnett-Hartman, Anna E. Coghill, Michael N. Passarelli, John A. Baron, Dennis J. Ahnen, and Aung Ko Win, “BRAF mutation status and survival after colorectal cancer diagnosis according to patient and tumor characteristics,” Cancer Epidemiology Biomarkers and Prevention, vol. 21, no. 10, pp. 1792–1798, 2012.
- N. F. C. C. de Miranda, F. J. Hes, T. van Wezel, and H. Morreau, “Role of the microenvironment in the tumourigenesis of microsatellite unstable and MUTYH-associated polyposis colorectal cancers,” Mutagenesis, vol. 27, no. 2, pp. 247–253, 2012.
- Justyna Klusek, Stanislaw Gluszek, and Jolanta Klusek, “Selected mutations with high risk of colorectal cancer,” Przeglad Gastroenterologiczny, vol. 7, no. 1, pp. 1–6, 2012.
- Matthias Kloor, Laura Staffa, Aysel Ahadova, and Magnus Knebel Doeberitz, “Clinical significance of microsatellite instability in colorectal cancer,” Langenbeck's Archives of Surgery, 2013.
- Pilar Garre, Lorena Martín, Inmaculada Bando, Alicia Tosar, Patricia Llovet, Julián Sanz, Atocha Romero, Miguel Hoya, Eduardo Díaz-Rubio, and Trinidad Caldés, “Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer,” Familial Cancer, 2013.
- Guillermo Aldave, Eva Pay, Francisco Queipo, Miguel Angel Idoate, and Jorge Guridi, “Metástasis de un adenocarcinoma prostático en tronco cerebral en el contexto de un síndrome de Muir-Torre,” Neurocirugía, vol. 24, no. 2, pp. 78–81, 2013.
- Paul J Barrow, Tara Clancy, and D Gareth Evans, “Key genetic considerations in the management of suspected hereditary colorectal cancer,” Colorectal Cancer, vol. 2, no. 1, pp. 31–41, 2013.
- Linghua Wang, and David A. Wheeler, “Genomic Sequencing for Cancer Diagnosis and Therapy,” Annual Review of Medicine, vol. 65, no. 1, pp. 33–48, 2014.
- Henry T. Lynch, Stephen J. Lanspa, Carrie L. Snyder, and Kristen M. Drescher, “Microsatellite instability, disease-free survival and role of tumour infiltrating lymphocytes (Invited editorial on ‘Predictors of disease-free survival in colorectal cancer with microsatellite instability: An AGEO multicenter study’),” European Journal of Cancer, 2015.
- Qi Liu, and Bing Zhang, “Integrative Omics Analysis Reveals Post-Transcriptionally Enhanced Protective Host Response in Colorectal Cancers with Microsatellite Instability,” Journal of Proteome Research, 2015.
- Iris N. Pardieck, Priscilla A. Jawahier, Marloes Swets, Cornelis J.H. van de Velde, and Peter J.K. Kuppen, “Novel avenues in immunotherapies for colorectal cancer,” Expert Review of Gastroenterology & Hepatology, pp. 1–16, 2015.
- Fabian Echterdiek, Jonas Janikovits, Laura Staffa, Meike Müller, Bernd Lahrmann, Monika Frühschütz, Benjamin Hartog, Nina Nelius, Axel Benner, Mirjam Tariverdian, Magnus von Knebel Doeberitz, Niels Grabe, and Matthias Kloor, “Low density of FOXP3-positive T cells in normal colonic mucosa is related to the presence of beta2-microglobulin mutations in Lynch syndrome-associated colorectal cancer,” OncoImmunology, pp. 00–00, 2015.
- Talia Wegman-Ostrosky, Nancy Reynoso Noverón, Sonia Ilana Mejía-Pérez, Thalía Estefania Sánchez-Correa, Rosa María Álvarez, Silvia Vidal-Millán, Bernardo Cacho, José Sánchez-Corona, Luis A.Herrera Montalvo, and Teresita Corona Vázquez, “Clinical prognostic factors in adults with astrocytoma: Historic cohort.,” Clinical Neurology and Neurosurgery, 2016.
- Päivi Peltomäki, “Update on Lynch syndrome genomics,” Familial Cancer, 2016.
- Gaurav Goyal, Tiffany Fan, and Peter Todd Silberstein, “Hereditary cancer syndromes: utilizing DNA repair deficiency as therapeutic target,” Familial Cancer, 2016.