Evidence map›Paper›PMID 31285959›Full record

ArticleAmerican journal of cancer research2019

Inhibition of cisplatin-resistant head and neck squamous cell carcinoma by combination of Afatinib with PD0325901, a MEK inhibitor.

Xiaofeng Lin, Jipei Liao, Zejia Yang, Xiaoxuan Fan, Kevin J Cullen, Long Chen, Hancai Dan

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Rapamycin and trametinib: a rational combination for treatment of NSCLC.International journal of biological sciences · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Mechanisms of resistance in head and neck cancer.American journal of cancer research · 2020
    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

7 authors at 2 institutions in 2 countries.

Xiaofeng LinMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine Baltimore, MD, USA.
Jipei LiaoMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine Baltimore, MD, USA.
Zejia YangMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine Baltimore, MD, USA.
Xiaoxuan FanMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine Baltimore, MD, USA.
Kevin J CullenMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine Baltimore, MD, USA.
Long ChenDepartment of Radiation Oncology, Cancer Hospital Affiliated with Guangxi Medical University Nanning, Guangxi, China.
Hancai DanMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine Baltimore, MD, USA.
University of Maryland, Baltimore · USGuangxi Medical University · CN

Funding

Inhibition of castration resistant prostate cancer by targeting of the IKKbeta/AR signalingR01CA212094 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI DAN, HANCAI · 2017 to 2021
$1.8M
The Role of IKK and NF-kappaB in Controlling mTOR Signaling and TSC ProgressionR00CA149178 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI DAN, HANCAI · 2013 to 2015
$709k
NCI NIH HHS R00 CA149178NCI NIH HHS R01 CA212094
6 · The paper itself

Abstract

ErbB family members that contain EGFR, HER2, HER3 and HER4 play important roles in many cancer types, including head and neck; however, inhibition of these receptors by small molecule kinase inhibitors showed limited results due to compensatory up-regulation of some key survival signaling pathways. Here, we explore the effectiveness of Afatinib, an irreversible inhibitor of EGFR, HER2, and HER4, in combination with the MEK inhibitor PD0325901 to inhibit cisplatin-resistant head and neck squamous cell carcinoma (HNSCC). We treated two cisplatin-resistant HNSCC cell lines, UMSCC74B and O28, with Afatinib, PD0325901, or a combination, and measured signaling pathways, cell proliferation, and survival. We found that Afatinib blocked Akt/mTOR activity and phosphorylation of EGFR, HER2 and HER3, but up-regulated MEK/ERK signaling. Interestingly, MEK inhibitor PD0325901 blocked ERK phosphorylation, but elevated phosphorylation of Akt and mTOR pathways. Similarly, Afatinib and PD0325901 inhibited all these pathways and synergistically suppressed cell proliferation and survival. Our data demonstrate that Afatinib in combination with MEK inhibitors could provide a potential novel therapy for cisplatin-resistant head and neck squamous cell cancer.

Indexed as

AfatinibAktcisplatin-resistant HNSCCEGFREGFR inhibitorsERKHead and neck squamous cell carcinomaHNSCCMEKMEK inhibitormTORPD0325901PI3K

Identifiers

PMID31285959
PMCPMC6610054
OpenAlexW2984237424

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.