Tumour cell dormancy as a contributor to the reduced survival of GBM patients who received standard therapy Article Swipe
Luqing Tong
,
Yi Li
,
Peidong Liu
,
Iruni Roshanie Abeysekera
,
Hai Long
,
Tao Li
,
Zhennan Tao
,
Haiwen Ma
,
Yang Xie
,
Yubao Huang
,
Shengping Yu
,
Jiabo Li
,
Feng Yuan
,
Xuejun Yang
·
YOU?
·
· 2018
· Open Access
·
· DOI: https://doi.org/10.3892/or.2018.6425
YOU?
·
· 2018
· Open Access
·
· DOI: https://doi.org/10.3892/or.2018.6425
Glioblastoma multiforme (GBM) is a fatal cancer with varying life expectancy, even for patients undergoing the same standard therapy. Identification of differentially expressed genes in GBM patients with different survival rates may benefit the development of effective therapeutic strategies. In the present study, key pathways and genes correlated with survival in GBM patients were screened with bioinformatic analysis. Included in the study were 136 eligible patients who had undertaken surgical resection of GBM followed by temozolomide (TMZ) chemoradiation and long-term therapy with TMZ. A total of 383 differentially expressed genes (DEGs) related to GBM survival were identified. Gene Ontology and pathway enrichment analysis as well as hub gene screening and module analysis were performed. As expected, angiogenesis and migration of GBM cells were closely correlated with a poor prognosis. Importantly, the results also indicated that cell dormancy was an essential contributor to the reduced survival of GBM patients. Given the lack of specific targeted genes and pathways known to be involved in tumour cell dormancy, we proposed enriched candidate genes related to the negative regulation of cell proliferation, signalling pathways regulating pluripotency of stem cells and neuroactive ligand-receptor interaction, and 3 hub genes (FTH1, GRM1 and DDIT3). Maintaining persistent cell dormancy or preventing tumour cells from entering dormancy during chemoradiation should be a promising therapeutic strategy.
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Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.3892/or.2018.6425
- http://www.spandidos-publications.com/10.3892/or.2018.6425/download
- OA Status
- bronze
- Cited By
- 19
- References
- 46
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W2802045597
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
-
https://openalex.org/W2802045597Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.3892/or.2018.6425Digital Object Identifier
- Title
-
Tumour cell dormancy as a contributor to the reduced survival of GBM patients who received standard therapyWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2018Year of publication
- Publication date
-
2018-05-08Full publication date if available
- Authors
-
Luqing Tong, Yi Li, Peidong Liu, Iruni Roshanie Abeysekera, Hai Long, Tao Li, Zhennan Tao, Haiwen Ma, Yang Xie, Yubao Huang, Shengping Yu, Jiabo Li, Feng Yuan, Xuejun YangList of authors in order
- Landing page
-
https://doi.org/10.3892/or.2018.6425Publisher landing page
- PDF URL
-
https://www.spandidos-publications.com/10.3892/or.2018.6425/downloadDirect link to full text PDF
- Open access
-
YesWhether a free full text is available
- OA status
-
bronzeOpen access status per OpenAlex
- OA URL
-
https://www.spandidos-publications.com/10.3892/or.2018.6425/downloadDirect OA link when available
- Concepts
-
Temozolomide, Biology, Cancer research, Dormancy, Cell cycle, Cancer, Cell, Oncology, Bioinformatics, Medicine, Glioma, Genetics, Germination, BotanyTop concepts (fields/topics) attached by OpenAlex
- Cited by
-
19Total citation count in OpenAlex
- Citations by year (recent)
-
2025: 1, 2024: 2, 2023: 2, 2022: 1, 2021: 5Per-year citation counts (last 5 years)
- References (count)
-
46Number of works referenced by this work
- Related works (count)
-
10Other works algorithmically related by OpenAlex
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| referenced_works | https://openalex.org/W2145814270, https://openalex.org/W2127970224, https://openalex.org/W1993497779, https://openalex.org/W2603523955, https://openalex.org/W2513196336, https://openalex.org/W2147000598, https://openalex.org/W2054733067, https://openalex.org/W2059346427, https://openalex.org/W1989041816, https://openalex.org/W2053363952, https://openalex.org/W2119605126, https://openalex.org/W1876708341, https://openalex.org/W2278244109, https://openalex.org/W1593855781, https://openalex.org/W2040158067, https://openalex.org/W2096937453, https://openalex.org/W2915401949, https://openalex.org/W2136875995, https://openalex.org/W1607460565, https://openalex.org/W2091477187, https://openalex.org/W2111940175, https://openalex.org/W1976078324, https://openalex.org/W2041036769, https://openalex.org/W2141222526, https://openalex.org/W2140286004, https://openalex.org/W2766037597, https://openalex.org/W2000432680, https://openalex.org/W2074749435, https://openalex.org/W2000285730, https://openalex.org/W2080100430, https://openalex.org/W2113758972, https://openalex.org/W2037236573, https://openalex.org/W2590066827, https://openalex.org/W4246844166, https://openalex.org/W2075239854, https://openalex.org/W2012900885, https://openalex.org/W2006986876, https://openalex.org/W4293529598, https://openalex.org/W1978041336, https://openalex.org/W2113399114, https://openalex.org/W2014119944, https://openalex.org/W2099478930, https://openalex.org/W2013767913, https://openalex.org/W2048711939, https://openalex.org/W1821696031, https://openalex.org/W2058901785 |
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