Familial aggregation of gastric cancer with microsatellite instability
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Polom, Karol
[1
,2
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Marrelli, Daniele
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Univ Siena, Dept Med Surg & Neurosci, Unit Gen Surg & Surg Oncol, Siena, ItalyUniv Siena, Dept Med Surg & Neurosci, Unit Gen Surg & Surg Oncol, Siena, Italy
Marrelli, Daniele
[1
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Voglino, Costantino
[1
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Roviello, Giandomenico
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Univ Trieste, Dept Med Surg & Hlth Sci, Trieste, Italy
San Donato Hosp, Dept Oncol, Med Oncol Unit, Arezzo, ItalyUniv Siena, Dept Med Surg & Neurosci, Unit Gen Surg & Surg Oncol, Siena, Italy
Roviello, Giandomenico
[3
,4
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De Franco, Lorenzo
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Univ Siena, Dept Med Surg & Neurosci, Unit Gen Surg & Surg Oncol, Siena, ItalyUniv Siena, Dept Med Surg & Neurosci, Unit Gen Surg & Surg Oncol, Siena, Italy
De Franco, Lorenzo
[1
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Vindigni, Carla
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Azienda Osped Univ Senese, Dept Pathol, Siena, ItalyUniv Siena, Dept Med Surg & Neurosci, Unit Gen Surg & Surg Oncol, Siena, Italy
Vindigni, Carla
[5
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Generali, Daniele
[3
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Roviello, Franco
[1
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[1] Univ Siena, Dept Med Surg & Neurosci, Unit Gen Surg & Surg Oncol, Siena, Italy
[2] Med Univ Gdansk, Dept Surg Oncol, Gdansk, Poland
Background: Microsatellite instability (MSI) is currently a new molecular subtype of gastric cancer (GC). About 90% of GC cases appear sporadically. MSI seems to be responsible for both sporadic and familial GC. The aim of this study was to analyze the frequency of MSI in GC with familial history of GC. Methods: The MSI analysis was conducted using five quasi-monomorphic mononucleotide repeats: BAT-26, BAT-25, NR-24, NR-21 and NR-27. From our database, we analyzed 457 patients in terms of cancer history across family members, particularly focusing on GC. Results: MSI status in patients without familial history of GC was present in 22.1% of the cases, whereas in the patients with familial history of GC it was present in 28% of the cases (p = 0.220). For 1st or 2nd degree family members with GC, MSI was observed in 27.6% and in 30.8%, respectively (p = 0.812). MSI was observed in hereditary gastric cancer (HGC) in 33.3% and in familial gastric cancer (FGC) in 30%. No difference in survival rates was observed between the analyzed groups. Conclusions: In our publication, we could not find any link between familial background and the MSI status in GC patients. More detailed molecular and genetic analysis of subgroups of these patients is required.
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Keimyung Univ, Dept Surg, Coll Med, Taegu, South KoreaKeimyung Univ, Sch Med, Dept Anat, Coll Med, Taegu, South Korea
Jeong, Chang-Wook
Lee, Jae-Ho
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机构:Keimyung Univ, Sch Med, Dept Anat, Coll Med, Taegu, South Korea
Lee, Jae-Ho
Sohn, Soo-Sang
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Keimyung Univ, Dept Surg, Coll Med, Taegu, South KoreaKeimyung Univ, Sch Med, Dept Anat, Coll Med, Taegu, South Korea
Sohn, Soo-Sang
Ryu, Seung-Wan
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Keimyung Univ, Dept Surg, Coll Med, Taegu, South KoreaKeimyung Univ, Sch Med, Dept Anat, Coll Med, Taegu, South Korea
Ryu, Seung-Wan
Kim, Dae-Kwang
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Keimyung Univ, Sch Med, Dept Anat, Coll Med, Taegu, South Korea
Keimyung Univ, Inst Med Genet, Coll Med, Taegu, South Korea
Hanvit Inst Med Genet, Taegu, South KoreaKeimyung Univ, Sch Med, Dept Anat, Coll Med, Taegu, South Korea