Evidence map›Paper›PMID 29749431›Full record

ArticleInternational journal of molecular medicine2018

Expression of annexin II and stromal tenascin C promotes epithelial to mesenchymal transition and correlates with distant metastasis in pancreatic cancer.

Naoko Yoneura, Shigetsugu Takano, Hideyuki Yoshitomi, Yasuyuki Nakata, Reiri Shimazaki, Shingo Kagawa, Katsunori Furukawa, Tsukasa Takayashiki, Satoshi Kuboki, Masaru Miyazaki and 1 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Biomarkers of tumor invasiveness in proteomics (Review).International journal of oncology · 2020
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. What is new in cancer-associated fibroblast biomarkers?Cell communication and signaling : CCS · 2023
    Review
  8. Article
  9. Article
  10. IGF1 receptor-targeted black TiOJournal of nanobiotechnology · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Annexin Animal Models-From Fundamental Principles to Translational Research.International journal of molecular sciences · 2021
    Review
  18. Review
  19. Review
  20. Review
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.

Naoko YoneuraDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Shigetsugu TakanoDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Hideyuki YoshitomiDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Yasuyuki NakataDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Reiri ShimazakiDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Shingo KagawaDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Katsunori FurukawaDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Tsukasa TakayashikiDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Satoshi KubokiDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Masaru MiyazakiDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Masayuki OhtsukaDepartment of General Surgery, Chiba University, Graduate School of Medicine, Chiba 260‑8677, Japan.
Chiba University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The interaction between cancer cells and stromal components contributes to cancer invasion and metastasis in pancreatic ductal adenocarcinoma (PDAC). The present study investigated the role of the correlation between annexin II (ANX2) and stromal tenascin C (TNC) with the progression of PDAC. The functions of the expression ANX2 and TNC were assessed in in vitro experiments using mouse and human PDAC cells, and the clinical effect was analyzed using immunohistochemistry with surgically resected PDAC tissues. The effects on epithelial to mesenchymal transition (EMT), invasion, putative cancer stemness, and anoikis resistance were examined in vitro using murine precancerous pancreatic intraepithelial neoplasia (PanIN) cells and murine and human invasive PDAC cells with ANX2 knockdown using specific small interfering RNA (siRNA)s and recombinant TNC (rTNC). ANX2 was expressed at a high level in primary PanIN cells and invasive PDAC cells, compared with the levels in liver metastatic PDAC cells. In the ANX2‑knockdown cells, there were fewer cells with a morphological mesenchymal appearance in three‑dimensional culture and invasion was reduced compared with that in the control cells. Morphological change into the mesenchymal phenotype and invasion were enhanced by rTNC treatment in the control PDAC cells but not in the ANX2‑knockdown cells. Pancreatosphere formation assays showed that ANX2 and TNC facilitated the maintenance of stem‑like characters in PDAC cells. Furthermore, anoikis assays indicated that the interaction of ANX2‑TNC contributed to anoikis resistance in PDAC cells. In the immunohistochemistry analyses, the group with a high expression of ANX2 and high stromal TNC was significantly correlated with distant metastasis, and was associated with hematogenous/peritoneal recurrence and poor outcomes following surgery in resected human primary PDAC tissues. In conclusion, the results demonstrated that ANX2 and stromal TNC regulated invasion in addition to stemness and anoikis resistance, which are crucial for metastasis in the progression of PDAC. These results indicate the potential of the ANX2‑TNC axis as a therapeutic target for PDAC metastasis.

Indexed as

Epithelial-Mesenchymal TransitionAgedAnimalsAnnexin A2AnoikisCarcinoma, Pancreatic DuctalFemaleHumansMaleMiceMiddle AgedNeoplasm InvasivenessNeoplasm MetastasisPancreatic NeoplasmsPrognosisProtein Interaction MapsAnnexin A2Tenascin

Identifiers

PMID29749431
PMCPMC6034933
OpenAlexW2801196557

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.