| First Author | Ha GH | Year | 2013 |
| Journal | Cancer Lett | Volume | 336 |
| Issue | 1 | Pages | 24-33 |
| PubMed ID | 23624299 | Mgi Jnum | J:198439 |
| Mgi Id | MGI:5496742 | Doi | 10.1016/j.canlet.2013.04.022 |
| Citation | Ha GH, et al. (2013) Transforming acidic coiled-coil proteins (TACCs) in human cancer. Cancer Lett 336(1):24-33 |
| abstractText | Fine-tuned regulation of the centrosome/microtubule dynamics during mitosis is essential for faithful cell division. Thus, it is not surprising that deregulations in this dynamic network can contribute to genomic instability and tumorigenesis. Indeed, centrosome loss or amplification, spindle multipolarity and aneuploidy are often found in a majority of human malignancies, suggesting that defects in centrosome and associated microtubules may be directly or indirectly linked to cancer. Therefore, future research to identify and characterize genes required for the normal centrosome function and microtubule dynamics may help us gain insight into the complexity of cancer, and further provide new avenues for prognostic, diagnostics and therapeutic interventions. Members of the transforming acidic coiled-coil proteins (TACCs) family are emerging as important players of centrosome and microtubule-associated functions. Growing evidence indicates that TACCs are involved in the progression of certain solid tumors. Here, we will discuss our current understanding of the biological function of TACCs, their relevance to human cancer and possible implications for cancer management. |
