Evidence map›Paper›PMID 27517322›Full record

ArticleOncotarget2016

Therapeutic implication of HER2 in advanced biliary tract cancer.

Ah-Rong Nam, Ji-Won Kim, Yongjun Cha, Hyerim Ha, Ji Eun Park, Ju-Hee Bang, Mei Hua Jin, Kyung-Hun Lee, Tae-Yong Kim, Sae-Won Han and 4 more

Open access · diamondAbstract readClinical Trial, Phase I
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 6% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Article
  4. Article
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  7. Review
  8. YAP as a therapeutic target to reverse trastuzumab resistance.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2025
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. HER2-targeted therapies beyond breast cancer - an update.Nature reviews. Clinical oncology · 2024
    Review
  15. Article
  16. Review
  17. Review
  18. Review
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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

14 authors at 3 institutions in 1 country.

Ah-Rong NamCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Ji-Won KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Yongjun ChaCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Hyerim HaDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Ji Eun ParkCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Ju-Hee BangCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Mei Hua JinCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Kyung-Hun LeeCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Tae-Yong KimCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Sae-Won HanCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Seock-Ah ImCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Tae-You KimCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Do-Youn OhCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Yung-Jue BangCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Seoul National University · KRSeoul National University Hospital · KRSeoul National University Bundang Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, there is no validated therapeutic target for biliary tract cancer (BTC). This study aimed to investigate the pre-clinical and clinical implication of HER2 as a therapeutic target in BTC. We established two novel HER2-amplified BTC cell lines, SNU-2670 and SNU-2773, from gallbladder cancer patients. SNU-2670 and SNU-2773 cells were sensitive to trastuzumab, dacomitinib, and afatinib compared with nine HER2-negative BTC cell lines. Dacomitinib and afatinib led to G1 cell cycle arrest in SNU-2773 cells and apoptosis in SNU-2670 cells. Furthermore, dacomitinib, afatinib, and trastuzumab showed synergistic cytotoxicity when combined with some cytotoxic drugs including gemcitabine, cisplatin, paclitaxel, and 5-fluorouracil. In a SNU-2670 mouse xenograft model, trastuzumab demonstrated a good anti-tumor effect as a monotherapy and in combination with gemcitabine increasing apoptosis. In our clinical data, 13.0% of patients with advanced BTC were defined as HER2-positive. Of these, three patients completed HER2-targeted chemotherapy. Two of them demonstrated a partial response, and the other one showed stable disease for 18 weeks. In summary, these pre-clinical and clinical data suggest that HER2 could be a therapeutic target, and that a HER2-targeting strategy should be developed further in patients with HER2-positive advanced BTC.

Indexed as

AdenocarcinomaAdultAgedAnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsApoptosisCell Line, TumorDrug Evaluation, PreclinicalErb-b2 Receptor Tyrosine KinasesFemaleFluorodeoxyglucose F18GallbladderGallbladder NeoplasmsGene AmplificationHumansAntineoplastic AgentsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFluorodeoxyglucose F18biliary tract cancergallbladder cancerHER2targeted therapytrastuzumab

Identifiers

PMID27517322
PMCPMC5295408
OpenAlexW2509178369

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.