Precursors of pancreatic cancer
Language English Country England, Great Britain Media print
Document type Journal Article, Review
- MeSH
- Early Detection of Cancer MeSH
- Carcinoma, Pancreatic Ductal genetics metabolism pathology therapy MeSH
- Epigenesis, Genetic MeSH
- Middle Aged MeSH
- Humans MeSH
- Cell Transformation, Neoplastic genetics metabolism pathology MeSH
- Biomarkers, Tumor genetics metabolism MeSH
- Pancreatic Neoplasms genetics metabolism pathology therapy MeSH
- Precancerous Conditions genetics metabolism pathology therapy MeSH
- Prognosis MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Risk Factors MeSH
- Aged MeSH
- Signal Transduction MeSH
- Animals MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Biomarkers, Tumor MeSH
Pancreatic cancer (PC) behaves very differently in comparison with other malignancies. Its incidence has been increasing continuously; mortality has not decreased, the diagnosis is frequently late, radical surgery is performed only in 15-20% of patients, and chemotherapy is only palliative. PC occurs in three different forms. Sporadic PC accounts for 90% of all PCs. Its most frequent form is the pancreatic ductal adenocarcinoma. The remaining 10% constitute two minority groups: familial PC (7%) and PC as a manifestation of a genetic cancer syndrome (3%). PCs are preceded by a precancerous lesion (precursor). At present, six different precursors are known. They have different histomorphological characteristics and malignant potential. The recognition and correct interpretation of individual precursors influences adequate clinical decision-making. The publication surveys the present knowledge of individual precursors and their role in the early pancreatic carcinogenesis.
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