Evidence map›Paper›PMID 26747179›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Upregulation of CD44v6 contributes to acquired chemoresistance via the modulation of autophagy in colon cancer SW480 cells.

Lin Lv, Hai-Guang Liu, Si-Yang Dong, Fan Yang, Qing-Xuan Wang, Gui-Long Guo, Yi-Fei Pan, Xiao-Hua Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
7.2field-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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. CD44 variant exons induce chemoresistance by modulating cell death pathways.Frontiers in cell and developmental biology · 2025
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Selection of Cancer Stem Cell-Targeting Agents Using Bacteriophage Display.Methods in molecular biology (Clifton, N.J.) · 2022
    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 2 institutions in 1 country.

Lin LvDepartment of Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Hai-Guang LiuDepartment of Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Si-Yang DongDepartment of Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Fan YangDepartment of Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Qing-Xuan WangDepartment of Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Gui-Long GuoDepartment of Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Yi-Fei PanDepartment of Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Xiao-Hua ZhangDepartment of Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China. zhangxhoncology@163.com.
Wenzhou Medical University · CNFirst Affiliated Hospital of Wenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CD44 isoform containing variant exon v6 (CD44v6) plays an important role in the progression, metastasis, and prognosis of colorectal cancer (CRC). Recently, it was found that CD44v6 is involved in acquired drug resistance. This study aimed to investigate the molecular mechanism of CD44v6 in the resistance of CRC cells to chemotherapy. A stable CD44v6 overexpression model in SW480 cells was established via lentiviral transduction. The chemosensitivity of cells to 5-fluorouracil (5-FU) and oxaliplatin (L-OHP) was determined by cell counting kit (CCK)-8, lactate dehydrogenase (LDH) release, and colony formation assays. Immunohistochemical staining of CD44v6 was performed in human CRC tissues. The key components in cell apoptosis, drug efflux and metabolism, mismatch repair, autophagy, epithelial-mesenchymal transition (EMT), and the PI3K-Akt and MAPK-Ras-Erk1/2 pathways were assessed using flow cytometry, quantitative real-time polymerase chain reaction (PCR), and western blot assays. The CD44v6 overexpression cells showed a higher viability, a lower LDH release rate, and an increased clonogenicity than the control cells under drug treatment. Moreover, overexpression of CD44v6 resulted in enhanced autophagy flux, EMT, and phosphorylation of Akt and Erk in the presence of drugs. Furthermore, high CD44v6 expression in the primary tumor was closely associated with an early recurrence in CRC patients who underwent curative surgery and adjuvant chemotherapy. In conclusion, overexpression of CD44v6 contributes to chemoresistance in SW480 cells under cytotoxic stress via the modulation of autophagy, EMT, and activation of the PI3K-Akt and MAPK-Ras-Erk pathways.

Indexed as

ApoptosisAutophagyCell Line, TumorColonic NeoplasmsDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionFluorouracilGenes, rasHumansHyaluronan ReceptorsMAP Kinase Signaling SystemMitogen-Activated Protein KinasesOrganoplatinum CompoundsOxaliplatinPhosphatidylinositol 3-KinasesPhosphorylationCD44 protein, humanFluorouracilHyaluronan ReceptorsMitogen-Activated Protein KinasesOrganoplatinum CompoundsOxaliplatinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAutophagyCD44v6ChemoresistanceColorectal cancer

Identifiers

PMID26747179
OpenAlexW2224158681

What OpenQuestion holds

Textmetadata
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.