Evidence map›Paper›PMID 18594980›Full record

ArticleDigestive diseases and sciences2009

siRNA directed against survivin enhances pancreatic cancer cell gemcitabine chemosensitivity.

Wen-Song Liu, Hai-Jiao Yan, Ren-Yi Qin, Rui Tian, Min Wang, Jian-Xin Jiang, Ming Shen, Cheng-Jian Shi

Abstract read
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In one paragraph

Article in Digestive diseases and sciences, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Paclitaxel tumor priming promotes delivery and transfection of intravenous lipid-siRNA in pancreatic tumors.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Article
  8. Article
  9. Article
  10. The emerging role of exosomes in survivin secretion.Histology and histopathology · 2015
    Review
  11. Article
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  13. Article
  14. The dual PI3K/mTOR inhibitor NVP-BGT226 induces cell cycle arrest and regulates Survivin gene expression in human pancreatic cancer cell lines.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2012
    Article
  15. Article
  16. Overcoming drug resistance in pancreatic cancer.Expert opinion on therapeutic targets · 2011
    Review
  17. Survivin and pancreatic cancer.World journal of clinical oncology · 2011
    Article
  18. Article
  19. Article
  20. 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

8 authors at 3 institutions in 1 country.

Wen-Song LiuDepartment of Biliary-Pancreatic Surgery, Affiliated Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Hai-Jiao Yan
Ren-Yi Qin
Rui Tian
Min Wang
Jian-Xin Jiang
Ming Shen
Cheng-Jian Shi
Huazhong University of Science and Technology · CNTongji Hospital · CNSun Yat-sen University Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Survivin is known to be overexpressed in various human malignancies, including pancreatic cancer, and to cause resistance to radiation and chemotherapy, so the regulation of this molecule could be a new strategy for treating pancreatic cancer. In our study, a short interfering RNA (siRNA) plasmid expression vector against survivin was constructed and transfected into human pancreatic cancer cell lines of Panc-1 and BxPC3. The expression of survivin mRNA and protein among the stable transfected cells and the untransfected cells was detected by semi-quantitative reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot, respectively. Tumor cell growth in vitro was assessed by trypan blue exclusion. The cell cycle distribution and cell apoptosis were measured by flow cytometry. The cytotoxicity assay was measured by the MTT test. Our results showed that survivin siRNA treatment caused a specific and profound decrease of survivin mRNA and protein that was associated with decreased cell growth, spontaneous apoptosis, and a specific G0/G1 arrest. Furthermore, the suppression of survivin can enhance the chemosensitivity of pancreatic cancer cells to gemcitabine significantly. We suggest that the RNAi against survivin gene strategy would be a potential approach to chemosensitization therapy in human pancreatic cancer.

Indexed as

AdenocarcinomaAntimetabolites, AntineoplasticApoptosisCell CycleCell Line, TumorCell ProliferationDeoxycytidineGemcitabineGene Expression Regulation, NeoplasticHumansInhibitor of Apoptosis ProteinsMicrotubule-Associated ProteinsPancreatic NeoplasmsPlasmidsRNA, Small InterferingSurvivinAntimetabolites, AntineoplasticBIRC5 protein, humanDeoxycytidineGemcitabineInhibitor of Apoptosis ProteinsMicrotubule-Associated ProteinsRNA, Small InterferingSurvivin

Identifiers

PMID18594980
OpenAlexW2025145816

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.