The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.
tRNA-derived fragments and tRNA halves: The new players in cancers
Abstract
tRNA-derived fragments (tRFs) and tRNA halves (tiRNAs) are small non-coding RNAs derived from precursor tRNAs or mature tRNAs. Depending on the sources, tRFs can be divided into tRF-1, tRF-2, tRF-3, tRF-5, and i-tRF; tiRNAs can be divided into 5'tiRNA and 3'tiRNA. Both tRFs and tiRNAs play important roles in tumorigenesis. Some tRFs and tiRNAs promote cell proliferation and cell cycle progression by regulating the expression of oncogenes. Other tRFs and tiRNAs inhibit cancer progression. Mechanism studies have shown that tRFs and tiRNAs may bind to RNA binding proteins such as Y-box binding protein 1 (YBX1) and prevent transcription, inactivate initiation factor eIF4G/A, promote translation of ribosomal proteins, or activate aurora kinase A, the regulator of mitosis. Therefore, tRFs and tiRNAs regulate the occurrence and development of cancers, including lung cancer, colorectal cancer, prostate cancer, breast cancer, ovarian cancer, B cell lymphoma, chronic lymphocytic leukemia, etc. This article reviews the classification of tRFs and tiRNAs, their biological functions in the occurrence of cancers, and their relationships with some common cancers. It will provide new ideas for the diagnosis and treatment of cancers.
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1 retracted
Critical Role of Notch Signaling in Osteosarcoma Invasion and Metastasis
Zhang, P., Yang, Y., Zweidler‐McKay, P. A., & Hughes, D. P. M. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-1992 · Cited by 154
RetractedInsights into RNA Biology from an Atlas of Mammalian mRNA-Binding Proteins
Castello, A., Fischer, B., Eichelbaum, K., Horos, R., Beckmann, B. M., Strein, C., Davey, N. E., Humphreys, D. T., Preiss, T., Steinmetz, L. M., et al. (2012) · Cell · doi:10.1016/j.cell.2012.04.031 · Cited by 2,132
Mapping the Human miRNA Interactome by CLASH Reveals Frequent Noncanonical Binding
Helwak, A., Kudla, G., Dudnakova, T., & Tollervey, D. (2013) · Cell · doi:10.1016/j.cell.2013.03.043 · Cited by 1,269
Angiogenin-Induced tRNA Fragments Inhibit Translation Initiation
Ivanov, P., Emara, M. M., Villen, J., Gygi, S. P., & Anderson, P. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.06.022 · Cited by 985
Endogenous tRNA-Derived Fragments Suppress Breast Cancer Progression via YBX1 Displacement
Goodarzi, H., Liu, X., Nguyen, H. C. B., Zhang, S., Fish, L., & Tavazoie, S. F. (2015) · Cell · doi:10.1016/j.cell.2015.02.053 · Cited by 949
Angiogenin cleaves tRNA and promotes stress-induced translational repression
Yamasaki, S., Ivanov, P., Hu, G.-F., & Anderson, P. (2009) · Journal of Cell Biology · doi:10.1083/jcb.200811106 · Cited by 936
Sphingosine 1-phosphate and cancer
Pyne, N. J., & Pyne, S. (2010) · Nature Reviews Cancer · doi:10.1038/nrc2875 · Cited by 852
Human tRNA-derived small RNAs in the global regulation of RNA silencing
Haussecker, D., Huang, Y., Lau, A., Parameswaran, P., Fire, A. Z., & Kay, M. A. (2010) · RNA · doi:10.1261/rna.2000810 · Cited by 713
Kumar, P., Anaya, J., Mudunuri, S. B., & Dutta, A. (2014) · BMC Biology · doi:10.1186/s12915-014-0078-0 · Cited by 643
Aberrant methylation of t RNA s links cellular stress to neuro‐developmental disorders
Blanco, S., Dietmann, S., Flores, J. V., Hussain, S., Kutter, C., Humphreys, P., Lukk, M., Lombard, P., Treps, L., Popis, M., et al. (2014) · The EMBO Journal · doi:10.15252/embj.201489282 · Cited by 620
Metadata
- Authors
- Zhu, L., Ge, J., Li, T., Shen, Y., & Guo, J.
- Venue
- Cancer Letters
- Publisher
- Elsevier BV
- Published
- 2019-06
- Volume
- 452
- Pages
- 31-37
- ISSN
- 0304-3835 (ISSN-L)
- OpenAlex
- W2924349232
- Cited by
- 256
- References
- 58
- FWCI
- 8.45
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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