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Pancreatic cancer is the third leading cause of cancer-related death in the United States. With a predicted five-year relative survival rate of 9%, pancreatic cancer continues to be clinically challenging due to its resistance to even the most aggressive combinations of surgery, chemotherapy, and radiotherapy. Because of indistinct symptoms and the absence of reliable diagnostic biomarkers, diagnoses are usually delayed and thus made when the disease is already advanced (which decreases five-year survival to less than 3%). Nevertheless, extensive research has highlighted the importance of several biomarkers and reagents that can significantly improve early detection.
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KRAS has the distinction of being a preeminent oncoprotein as it is mutated in nearly all pancreatic ductal adenocarcinomas (PDAC), with KRAS G12D and G12V mutations representing 75% of these changes (1). GeneTex’s RAS (G12D Mutant) monoclonal antibody [HL10] (GTX635362) is the first commercially available recombinant rabbit antibody that demonstrates exceptional sensitivity and specificity for the RAS G12D mutant protein in samples from human pancreatic cancer cell lines and a mouse model of PDAC by western blot (WB) and immunohistochemistry (IHC-P), respectively (Figure 1).
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Figure 1. GeneTex's recombinant rabbit RAS (G12D mutant) antibody [HL10] (GTX635362) is sensitive and specific for the RAS G12D mutation by WB and IHC-P in human pancreatic cancer cell lines and a PDAC mouse model.。
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Carbohydrate antigen 19-9 (CA19-9), also known as sialyl-LewisA, is a tetrasaccharide with the sequence Neu5Acα2-3Galβ1-3[Fucα1-4]GlcNAcβ. It is used clinically to assist in the diagnosis of pancreatic cancer, but is more widely used to monitor therapy and detect recurrences in diagnosed cases. CA19-9 is also elevated in many other diseases, including cholangiocarcinoma, colorectal cancer, hepatocellular carcinoma, and cirrhosis (2). GeneTex’s CA19-9 antibody [GT933] (GTX635389) showed superior sensitivity for WB, IHC-P, and immunocytochemistry (ICC/IF) in comparative testing against other well-known antibodies (Figures 2 & 3).
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Figure 2. GeneTex’s CA19-9 antibody [GT933] (GTX635389) generates a robust signal for IHC-P and WB in comparison to other antibodies.。
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Figure 3. GeneTex’s CA19-9 antibody [GT933] (GTX635389) demonstrates superior sensitivity for ICC/IF on SW1116 cells (high CA19-9 expression) and HT29 cells (low CA19-9 expression) in comparison to other antibodies.。
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Thrombospondin 2 (THBS2) is a secreted glycoprotein that can be expressed together with CA19-9 in patients with early pancreatic ductal adenocarcinoma (PDAC) (3). GeneTex offers a selection of antibody reagents for THBS2 research. Several of these are able to detect secreted protein in conditioned media from human AsPC-1 pancreatic tumor cells by WB. In addition, some of the antibodies clearly recognize THBS2 in human pancreatic tumor tissue samples by IHC-P (Figure 4).
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Figure 4. GeneTex’s Thrombospondin 2 polyclonal antibody (GTX134554) is validated for both WB and IHC-P (left), while the monoclonal antibody [GT7511] (GTX635392) is validated for WB (right).
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Glypican-1 expression is upregulated in many human malignancies, including pancreatic cancer (4). There is ongoing research into the potential clinical utility of assessing enriched glypican-1 expression on circulating exosomes as an early cancer marker. GeneTex proudly offers an outstanding, well-cited antibody specific for glypican-1 that has been thoroughly validated for WB, ICC/IF, IHC-P, FACS, IP, and ELISA (Figure 5).
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Figure 5. Glypican-1 antibody [N3C3] (GTX104557) detects glycosylated glypican-1 protein in various cell lines by WB and performs well in FACS.
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Though CA19-9 is the most familiar tumor marker associated with pancreatic cancer, there is ongoing interest in developing pancreatic cancer marker panels that include other proteins, glycoproteins, and microRNAs.
Table: Markers associated with pancreatic cancer
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References:
- Cold Spring Harb Perspect Med. 2018 Sep 4;8(9):a031435.
- J Gastrointest Oncol. 2012 Jun;3(2):105-19.
- Sci Transl Med. 2017 Jul 12;9(398):eaah5583.
- Ann Transl Med. 2016 Feb;4(4):64.