Evidence map›Paper›PMID 31616187›Full record

ArticleCancer management and research2019

Long non-coding RNA NNT-AS1 functions as an oncogenic gene through modulating miR-485/BCL9 in cholangiocarcinoma.

Lining Huang, Xingming Jiang, Pengcheng Kang, Zhidong Wang, Kaiming Leng, Daolin Ji, Yi Xu, Hao Wang, Yunfu Cui

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Long Non-Coding RNAs as Molecular Biomarkers in Cholangiocarcinoma.Frontiers in cell and developmental biology · 2022
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Cholangiocarcinoma: novel therapeutic targets.Expert opinion on therapeutic targets · 2020
    Review
  12. Article
  13. Article
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

9 authors at 1 institution in 1 country.

Lining Huang *Department of HPB Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150086, People's Republic of China.ORCID 0000-0003-1177-4530
Xingming Jiang *Department of HPB Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150086, People's Republic of China.
Pengcheng KangDepartment of HPB Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150086, People's Republic of China.
Zhidong WangDepartment of HPB Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150086, People's Republic of China.
Kaiming LengDepartment of HPB Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150086, People's Republic of China.
Daolin JiDepartment of HPB Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150086, People's Republic of China.
Yi XuDepartment of HPB Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150086, People's Republic of China.
Hao WangDepartment of HPB Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150086, People's Republic of China.
Yunfu CuiDepartment of HPB Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150086, People's Republic of China.
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGrowing evidence suggests that long non-coding RNAs (lncRNAs) could function as important regulators in carcinogenesis and cancer progression. Nicotinamide nucleotide transhydrogenase antisense RNA 1 (lncRNA NNT-AS1) is up-regulated in some human tumors and functions as a tumor promoter. This study aimed to detect the effect of NNT-AS1 on cholangiocarcinoma (CCA) prognosis. MATERIALS AND

methodsIn this study, we detected NNT-AS1 expression in CCA tissue samples and cell lines, and analyzed the association between NNT-AS1 expression levels and clinical parameters of CCA patients. Moreover, we conducted loss-of-function studies in CCA cancer cells to explore the biological function and molecular mechanism of NNT-AS1. NNT-AS1 was downregulated by using RNAi technology. Cell proliferation was examined by CCK8 and clone formation assays. Cell migration and invasion were determined by wound healing and transwell assays. Western blot assays were used to explore protein expression.

resultsIn this study, NNT-AS1 was expressed at high levels in CCA and closely associated with poor prognosis of patients with CCA. NNT-AS1 knockdown impaired cell proliferation, suppressed CCA cell migration and invasion, and restrained tumor growth in vitro. Moreover, NNT-AS1 directly bounded to miR-485 and further regulated BCL9. Finally, rescue assays verified that NNT-AS1 modulated the tumorigenesis of CCA by regulating miR-485.

conclusionTaken together, NNT-AS1 played a critical biological role in the development of CCA. Our results elucidated NNT-AS1/miR-485/BCL9 axis might lead to a further understanding of the molecular mechanism of CCA.

Indexed as

BCL9cholangiocarcinomalncRNANNT-AS1

Identifiers

PMID31616187
PMCPMC6699498
OpenAlexW2968995424

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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 OpenQuestion graph.