The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Serum YKL-40, A New Prognostic Biomarker in Cancer Patients?
Abstract
YKL-40, a member of the “mammalian chitinase–like proteins,” is expressed and secreted by several types of solid tumors. The exact function of YKL-40 in cancer diseases is unknown and is an important objective of future studies. YKL-40 exhibits growth factor activity for cells involved in tissue remodeling processes. YKL-40 may have a role in cancer cell proliferation, survival, and invasiveness, in the inflammatory process around the tumor, angiogenesis, and remodeling of the extracellular matrix. YKL-40 is neither organ- nor tumor-specific. However, the present retrospective clinical studies of patients with eight different types of primary or advanced solid tumors suggest that serum concentration of YKL-40 may be a new biomarker in cancer patients used as a “prognosticator.” Elevated serum YKL-40 is found in a subgroup of patients with different types of solid tumors, including several types of adenocarcinomas, small cell lung carcinoma, glioblastoma, and melanoma. The highest serum YKL-40 is detected in patients with advanced cancer and with the poorest prognosis. In many cases, serum YKL-40 provides independent information of survival. Serum YKL-40 cannot be used as a single screening test for cancer. The use of serum YKL-40 has not received Food and Drug Administration approval for use as a biomarker for cancer or any other disease. Large multicenter retrospective and prospective studies of patients with different types of cancer are required to determine: (a) if serum YKL-40 is a useful prognostic cancer biomarker, (b) if serum YKL-40 can be of value in monitoring patients with cancer in order to provide information about metastases before these are detected by routine methods, and (c) if serum YKL-40 can be useful for screening of cancer together with a panel of other cancer biomarkers and imaging techniques. (Cancer Epidemiol Biomarkers Prev 2006;15(2):194–202)
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Tumors: Wounds That Do Not Heal
Flier, J. S., Underhill, L. H., & Dvorak, H. F. (1986) · New England Journal of Medicine · doi:10.1056/nejm198612253152606 · Cited by 4,391 · cited 5×
“Primary breast cancer 271 57*** (22-688) 19 Johansen et al.”
BackgroundInfluentialBingle, L., Brown, N. J., & Lewis, C. E. (2002) · The Journal of Pathology · doi:10.1002/path.1027 · Cited by 2,022
New families in the classification of glycosyl hydrolases based on amino acid sequence similarities
Henrissat, B., & Bairoch, A. (1993) · Biochemical Journal · doi:10.1042/bj2930781 · Cited by 1,974
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Role of Chitin and Chitinase/Chitinase-Like Proteins in Inflammation, Tissue Remodeling, and Injury
Lee, C. G., Da Silva, C. A., Dela Cruz, C. S., Ahangari, F., Ma, B., Kang, M.-J., He, C.-H., Takyar, S., & Elias, J. A. (2011) · Annual Review of Physiology · doi:10.1146/annurev-physiol-012110-142250 · Cited by 896
Chitinases: in agriculture and human healthcare
Nagpure, A., Choudhary, B., & Gupta, R. K. (2014) · Critical Reviews in Biotechnology · doi:10.3109/07388551.2013.790874 · Cited by 145
Baldacci, F., Lista, S., Cavedo, E., Bonuccelli, U., & Hampel, H. (2017) · Expert Review of Proteomics · doi:10.1080/14789450.2017.1304217 · Cited by 113
YKL-40 IDENTIFIED BY PROTEOMIC ANALYSIS AS A BIOMARKER OF SEPSIS
Hattori, N., Oda, S., Sadahiro, T., Nakamura, M., Abe, R., Shinozaki, K., Nomura, F., Tomonaga, T., Matsushita, K., Kodera, Y., et al. (2009) · Shock · doi:10.1097/shk.0b013e31819e2c0c · Cited by 83
Diurnal, weekly, and long-time variation in serum concentrations of YKL-40 in healthy subjects
Johansen, J. S., Lottenburger, T., Nielsen, H. J., Jensen, J. E. B., Svendsen, M. N., Kollerup, G., & Christensen, I. J. (2008) · Cancer Epidemiology, Biomarkers & Prevention · doi:10.1158/1055-9965.epi-07-2766 · Cited by 72
Self-citationSerum YKL-40 levels are altered in endometriosis
Tuten, A., Kucur, M., Imamoglu, M., Oncul, M., Acikgoz, A. S., Sofiyeva, N., Ozturk, Z., Kaya, B., & Oral, E. (2014) · Gynecological Endocrinology · doi:10.3109/09513590.2014.887671 · Cited by 17
Metadata
- Authors
- Johansen, J. S., Jensen, B. V., Roslind, A., Nielsen, D., & Price, P. A.
- Venue
- Cancer Epidemiology, Biomarkers & Prevention
- Published
- 2006-02-01
- Volume
- 15
- Issue
- 2
- Pages
- 194-202
- ISSN
- 1055-9965 (ISSN-L)
- 1538-7755
- OpenAlex
- W2107332877
- Cited by
- 339
- References
- 3
- FWCI
- 8.22
- Type
- journal article
- Language
- en
- Open access
- closed
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