Evidence map›Paper›PMID 31196027›Full record

ArticleBMC cancer2019

CDCA2 promotes the proliferation of colorectal cancer cells by activating the AKT/CCND1 pathway in vitro and in vivo.

Yifei Feng, Wenwei Qian, Yue Zhang, Wen Peng, Jie Li, Qiou Gu, Dongjian Ji, Zhiyuan Zhang, Qingyuan Wang, Dongsheng Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
6.3field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. The role of theTranslational cancer research · 2026
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  3. Overexpression ofInternational journal of molecular sciences · 2025
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  4. Article
  5. CDCA4 promotes bladder cancer progression by JAK/STAT signaling pathway.Journal of cancer research and clinical oncology · 2025
    Article
  6. Article
  7. [Overexpression of CDHR2 inhibits proliferation of breast cancer cells by inhibiting the PI3K/Akt pathway].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Yifei FengDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029, Jiangsu, China.
Wenwei QianThe First School of Clinical Medicine, Nanjing Medical University, Nanjing, Jiangsu, China.
Yue ZhangDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029, Jiangsu, China.
Wen PengThe First School of Clinical Medicine, Nanjing Medical University, Nanjing, Jiangsu, China.
Jie LiThe First School of Clinical Medicine, Nanjing Medical University, Nanjing, Jiangsu, China.
Qiou GuThe First School of Clinical Medicine, Nanjing Medical University, Nanjing, Jiangsu, China.
Dongjian JiThe First School of Clinical Medicine, Nanjing Medical University, Nanjing, Jiangsu, China.
Zhiyuan ZhangThe First School of Clinical Medicine, Nanjing Medical University, Nanjing, Jiangsu, China.
Qingyuan WangThe First School of Clinical Medicine, Nanjing Medical University, Nanjing, Jiangsu, China.
Dongsheng ZhangDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029, Jiangsu, China.
Yueming SunDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029, Jiangsu, China. jssym@vip.sina.com.ORCID http://orcid.org/0000-0002-0543-134X
Jiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCell division cycle associated 2 (CDCA2), upregulated in lung adenocarcinoma and oral squamous cell carcinoma, may be related to some malignant diseases. Nevertheless, its role in colorectal cancer (CRC) remains unknown.

methodsCDCA2 expression was analyzed using The Cancer Genome Atlas (TCGA), quantitative real-time PCR (qRT-PCR), and immunohistochemistry. The impact of CDCA2 on cell proliferation was analyzed via loss- or gain-of-function assays. Furthermore, gene set enrichment analysis was conducted to explore the potential mechanism of CDCA2 in CRC. Lastly, the expression levels of CCND1 and AKT were measured in CRC cell lines.

resultsOur study revealed that CDCA2 expression was associated with tumor progression. Through loss- or gain-of-function assays, we found that upregulation of CDCA2 promoted the proliferation of DLD-1 cells, however, downregulation of CDCA2 in SW480 cells restrained proliferative capacity both in vitro and in vivo. The results of flow cytometry showed that CDCA2 promoted cell cycle progression via upregulation of CCND1 in CRC cell lines. In the following experiments, we found that CDCA2 regulated CCND1 expression through activating the PI3K/AKT pathway, and confirmed this using a specific PI3K inhibitor (LY294002).

conclusionsThis study demonstrates that overexpression of CDCA2 might target CCND1 to promote CRC cell proliferation and tumorigenesis through activation of the PI3K/AKT pathway.

Indexed as

AnimalsCarcinogenesisCarrier ProteinsCell Cycle ProteinsCell Line, TumorCell ProliferationChromonesColorectal NeoplasmsCyclin D1FemaleHumansMaleMiceMiddle AgedMorpholinesNuclear Proteins2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneCarrier ProteinsCDCA2 protein, humanCell Cycle ProteinsChromonesCyclin D1MorpholinesNuclear ProteinsPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsProto-Oncogene Proteins c-aktRNA, Small InterferingCCND1CDCA2Colorectal cancerPI3K/AKT pathwayProliferation

Identifiers

PMID31196027
PMCPMC6567669
OpenAlexW2949469310

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.