Abstract:Background/Aims: Many tumor markers have been utilized in the follow-up care of colorectal cancer patients. No marker, however, has proven reliably accurate in detecting recurrent disease. Methods: The strengths and weaknesses of currently available tumor markers are reviewed, with attention to related cost and efficacy. Results: Tumor antigens, enzymes, and genetic markers have been used as tumor markers. CEA and CA 19.9 are the most widely utilized; however, genetic markers are the most promising for the fut… Show more
“…During recent years, there have been many studies to define the biological profile of CRC to improve early diagnosis and the prognostic stratification, and eventually find a cure (Pokorny et al, 2000;Crawford et al, 2003). However, the biological factors involved in the development of CRC are not yet clear (Petrova et al, 2008;Campa et al, 2012).…”
These results suggest that the VEGF polymorphisms might play a role in the development of CRC. Therefore, the VEGF polymorphisms might be further investigated to use in the determination of risk factors for CRC and to have a predictive value for anti-VEGF-targeted cancer therapies.
“…During recent years, there have been many studies to define the biological profile of CRC to improve early diagnosis and the prognostic stratification, and eventually find a cure (Pokorny et al, 2000;Crawford et al, 2003). However, the biological factors involved in the development of CRC are not yet clear (Petrova et al, 2008;Campa et al, 2012).…”
These results suggest that the VEGF polymorphisms might play a role in the development of CRC. Therefore, the VEGF polymorphisms might be further investigated to use in the determination of risk factors for CRC and to have a predictive value for anti-VEGF-targeted cancer therapies.
“…[1][2][3][4][5][6] Continuously raised preoperative p-CEA levels are associated with an increased likelihood of recurrence and decreased survival. 7 Furthermore, postoperative p-CEA levels are useful as a monitor for the early detection of recurrence after curative surgery and for assessing response to chemotherapy in metastatic colorectal cancer.…”
There was virtually no change between preoperative p-CEA and d-CEA levels. These findings suggest that the d-CEA level is not a predictor for metachronous hepatic metastasis and that measuring p-CEA levels is sufficient in the surveillance of colorectal cancer.
“…During the last few years, many attempts have been made to define the biological profile of CRC in order to improve early diagnosis and the prognostic stratification, and eventually find a cure (2, 3). Although many biological factors have been implicated in the development of CRC, a clinical relevance has not yet been reached for most of them.…”
Since vascular endothelial growth factor (VEGF) is known to be a potent pro-angiogenic factor, we evaluated the potential association of two VEGF gene polymorphisms (-634G>C and 936C>T) with the susceptibility and the clinicopathologic characteristics of colorectal cancer (CRC). The VEGF genotypes were determined using fresh colorectal tissue from 465 patients who had undergone a surgical resection and peripheral blood lymphocytes from 413 healthy controls by PCR/DHPLC assay. For the -634G>C polymorphism, the -634 GC or CC genotype was associated with a decreased risk of CRC (odds ratio [OR], 0.62; p=0.001) as a dominant model of C allele, whereas the 936 TT genotype correlated with advanced stage/ metastasis, a high serum level of CA19-9, and an higher grade in patients with CRC. In the haplotype analyses, haplotype -634C/936C and -634G/936T were associated with a decreased susceptibility of CRC (OR, 0.53 and 0.56; p<0.001, respectively). These observations imply that the VEGF gene polymorphisms may be associated with the susceptibility or clinicopathologic features of CRC. However, further studies of other VEGF sequence variants and their biological functions are needed to understand the role of the VEGF gene polymorphisms in the development and progression of CRC.
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