Col11a1 Antibody
Source Reactivity Background References- Product Name
- Col11a1 Antibody
- Chemical Name
- Col11a1 Antibody
- Synonyms
- Col11a1 Antibody
- CBNumber
- CB35725565
- Formula Weight
- 0
- MOL File
- Mol file
Col11a1 Antibody Chemical Properties,Usage,Production
Source
Rabbit
Reactivity
Human
Background
The Extracellular Matrix is a complex network of macromolecules that provides structural tissue support to cells in the basement membrane and interstitial matrix. It is composed of many molecules, including proteins, glycoproteins, proteoglycans, and polysaccharides. One of the major proteins that comprise the ECM, and the human body, is collagen. Collagens are a large family of proteins. They are trimeric molecules composed of three alpha polypeptide chains that form a triple helix structure that is characteristic of all collagens. The large family of collagens is divided into three subgroups: the fibrillar collagens, the non-fibril forming collagens, and the fibril-associated collagens. These subgroups differ in their structure and supramolecular assembly.Collagen11A1 is a minor fibrillar collagen that is not normally expressed at high levels in most normal tissues with the exception of cartilage, where it is expressed in high levels, and some other tissues/ organs, where it is expressed at a lower level. However, it has been reported that the expression of this molecule is correlated with advanced tumorigenic disease through meta analysis of data from multiple cancers, including ovarian, colon, breast, and lung. Additionally, it has also been associated with epithelial-mesenchymal transition and metastasis. Cancer associated fibroblasts are typically the most abundant cell type in the stroma of many solid tumors. They are thought to contribute to ECM stiffness, which is ultimately thought to contribute to tumor growth and resistance to chemotherapeutic intervention. COL11A1 has been found to be elevated in CAFs and may contribute to chemotherapy resistance.
References
[1] Barkan, D. et al. (2010) Eur J Cancer 46, 1181-8.
[2] Hynes, R.O. (2009) Science 326, 1216-9.
[3] Ricard-Blum, S. (2011) Cold Spring Harb Perspect Biol 3, a004978.
[4] Yoshioka, H. et al. (1995) Dev Dyn 204, 41-7.
[5] Kim, H. et al. (2010) BMC Med Genomics 3, 51.
[6] Cheon, D.J. et al. (2014) Clin Cancer Res 20, 711-23.
[7] Fuentes-Martínez, N. et al. (2015) Histol Histopathol 30, 87-93.
[8] Sok, J.C. et al. (2013) Br J Cancer 109, 3049-56.
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