| Literature DB >> 29274322 |
Saied Mirshahidi1, Alfred Simental2, Steve C Lee2, Pedro A De Andrade Filho2, Nathaniel R Peterson2, Wenlong Cao2, Rosalia de Necochea-Campion3, Hao Yang4, Penelope Duerksen-Hughes5, Xiangpeng Yuan6.
Abstract
Papillary thyroid carcinoma (PTC) is the most common form of thyroid cancer and while it has a generally good prognosis, tumor recurrence remains a major clinical challenge. Studying laboratory cell lines as well as clinical specimens indicate that PTC may follow the cancer stem cell (CSC) model. However, CSC characteristics relevant in PTC initiation and progression remain largely unknown. Here we studied a population of sphere-growing tumor cells isolated from primary cultures of clinical PTC. These sphere-growing cells consisted of aldehyde dehydrogenase positive (ALDH+) and ALDH negative (ALDH-) cell subpopulations and demonstrated a hierarchical pattern of cell division. Using combinations of selective depletion, specific inhibition and cell sorting, we found that both subpopulations of the sphere cells were able to self-renew and initiate xenograft tumors independently, and fulfilled the definition of CSC. Importantly, when the subpopulations functioned together, the cancer-initiation efficiency and the xenograft tumor progression were significantly enhanced compared to either subpopulation alone. These data revealed crucial roles of ALDH- CSC in PTC biology and suggested that CSC subpopulations function cooperatively to control PTC initiation and progression. Together, our study indicates that CSC subpopulations isolated from clinical specimens offer unprecedented opportunities for investigating PTC pathogenesis and developing effective therapies.Entities:
Keywords: Aldehyde dehydrogenase; Cancer stem cells; Patient-derived xenograft tumor; Primary cells; Subpopulations of cancer stem cells; Thyroid carcinoma
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Year: 2017 PMID: 29274322 DOI: 10.1016/j.yexcr.2017.12.017
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905