Evidence map›Paper›PMID 37409635›Full record

ArticleCancer medicine2023

Umbelliprenin induces autophagy and apoptosis while inhibits cancer cell stemness in pancreatic cancer cells.

Hongcheng Wang, Yongzhi Liu, Yiwei Wang, Ting Xu, Guanggai Xia, Xinyu Huang

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Coumarins fromOncoTargets and therapy · 2025
    Article
  9. Review
  10. The role of autophagy in pancreatic diseases.Frontiers in pharmacology · 2024
    Review
  11. Sesquiterpenes and Sesquiterpene Derivatives fromAntioxidants (Basel, Switzerland) · 2023
    Review
  12. 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

6 authors at 2 institutions in 1 country.

Hongcheng WangDepartment of Hepatobiliary and Pancreatic Surgery, Sixth People's Hospital Affiliated Shanghai Jiao Tong University, Shanghai, China.
Yongzhi LiuAffiliated Xiaoshan Hospital Hangzhou Normal University, Zhejiang, China.
Yiwei WangDepartment of Hepatobiliary and Pancreatic Surgery, Sixth People's Hospital Affiliated Shanghai Jiao Tong University, Shanghai, China.
Ting XuDepartment of Hepatobiliary and Pancreatic Surgery, Sixth People's Hospital Affiliated Shanghai Jiao Tong University, Shanghai, China.
Guanggai XiaDepartment of Hepatobiliary and Pancreatic Surgery, Sixth People's Hospital Affiliated Shanghai Jiao Tong University, Shanghai, China.
Xinyu HuangDepartment of Hepatobiliary and Pancreatic Surgery, Sixth People's Hospital Affiliated Shanghai Jiao Tong University, Shanghai, China.ORCID 0000-0001-5976-1988
Shanghai Jiao Tong University · CNAffiliated Hospital of Hangzhou Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUmbelliprenin is a sesquiterpene coumarin isolated from Artemisia absinthium L. and shows antitumor effects in various cancers by inducing apoptosis. However, the antitumor effect of umbelliprenin in human pancreatic cancer has not been clarified.

methodsThe antitumor effects were determined by MTT and AnnexinV/PI double staining assay in vitro and xenograft mice in vivo. Autophagy was determined via immunofluorescence analysis. Apoptotic or autophagic related proteins were measured by immunoblotting. The pancreatic cancer cell stemness were determined by mammosphere formation and ALDEFLUOR assay.

resultsIt revealed that umbelliprenin inhibited pancreatic cancer cell proliferation in vitro and pancreatic cancer tumor growth in vivo. Moreover, umbelliprenin induced pancreatic cancer cell BxPC3 apoptosis and autophagy as evidenced by upregulated apoptosis and autophagy- related protein expression (p < 0.01). Blocking autophagy by 3-MA or Atg7 knockout enhanced umbelliprenin-induced apoptosis (p < 0.05). Umbelliprenin also reduced pancreatic cancer cell stemness by reducing Oct4, Nanog, and Sox2 mRNA levels (p < 0.01). Mechanistically, umbelliprenin greatly inhibited Akt/mTOR and Notch1 signal pathway.

conclusionUmbelliprenin may be a novel therapeutic approach for pancreatic cancer treatment.

Indexed as

ApoptosisPancreatic NeoplasmsAnimalsAutophagyCell Line, TumorCell ProliferationHumansMiceProto-Oncogene Proteins c-aktUmbelliferonesXenograft Model Antitumor AssaysProto-Oncogene Proteins c-aktUmbelliferonesumbellipreninAkt/mTOR signaling pathwayapoptosisautophagycancer stem cellspancreatic cancer

Identifiers

PMID37409635
PMCPMC10417289
OpenAlexW4383302191

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.