Evidence map›Paper›PMID 32399432›Full record

ArticleLiver cancer2020

Gene Signature for Sorafenib Susceptibility in Hepatocellular Carcinoma: Different Approach with a Predictive Biomarker.

Chang Min Kim, Shin Hwang, Bhumsuk Keam, Yun Suk Yu, Ji Hoon Kim, Dong-Sik Kim, Si Hyun Bae, Gun-Do Kim, Jong Kyu Lee, Yong Bae Seo and 6 more

Open access · goldAbstract read
In one paragraph

Article in Liver cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

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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

16 authors at 10 institutions in 2 countries.

Chang Min KimCbsBioscience Inc., Daejeon, Republic of Korea.
Shin HwangDivision of Hepatobiliary Surgery and Liver Transplantation, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Bhumsuk KeamDepartment of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
Yun Suk YuCbsBioscience Inc., Daejeon, Republic of Korea.
Ji Hoon KimDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Republic of Korea.
Dong-Sik KimDivision of HBP Surgery and Liver Transplantation, Department of Surgery, Korea University College of Medicine, Seoul, Republic of Korea.
Si Hyun BaeDepartment of Internal Medicine, Eunpyeong St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Gun-Do KimCbsBioscience Inc., Daejeon, Republic of Korea.
Jong Kyu LeeCbsBioscience Inc., Daejeon, Republic of Korea.
Yong Bae SeoCbsBioscience Inc., Daejeon, Republic of Korea.
Soon Woo NamDepartment of Internal Medicine, Incheon St. Mary's Hospital, The Catholic University of Korea, Incheon, Republic of Korea.
Koo Jeong KangDivision of Hepatobiliary and Pancreatic Surgery, Department of Surgery, Keimyung University Dong-San Medical Center, Daegu, Republic of Korea.
Luigi BuonaguroLaboratory of Cancer Immunoregulation, Instituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione G. Pascale" - IRCCS, Naples, Italy.
Jin Young ParkCbsBioscience Inc., Daejeon, Republic of Korea.
Yun Soo KimDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of Korea.
Hee Jung WangDepartment of Surgery, Ajou University School of Medicine, Suwon, Republic of Korea.
Korea University · KRAjou University · KRAsan Medical Center · KRCatholic University of Korea · KRGachon University · KRIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITKeimyung University · KRPukyong National University · KRSeoul National University Hospital · KRThe Catholic University of Korea Incheon St. Mary's Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimUniform treatment of hepatocellular carcinoma (HCC) with molecular targeted drugs (e.g., sorafenib) results in a poor overall tumor response when tumor subtyping is absent. Patient stratification based on actionable gene expression is a method that can potentially improve the effectiveness of these drugs. Here we aimed to identify the clinical application of actionable genes in predicting response to sorafenib.

methodsThrough quantitative real-time reverse transcription PCR, we analyzed the expression levels of seven actionable genes (

resultsThe responders had significantly higher TBS values than the nonresponders. With an area under the curve of 0.779, a TBS combining

conclusionsOur findings on patient stratification based on actionable molecular subtyping potentially provide a therapeutic strategy for improving sorafenib's effectiveness in treating HCC.

Indexed as

BiomarkerGene signatureHepatocellular carcinomaSorafenib

Identifiers

PMID32399432
PMCPMC7206603
OpenAlexW3008024136

What OpenQuestion holds

Textmetadata
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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.