Evidence map›Paper›PMID 39341920›Full record

ArticleAnnals of surgical oncology2025

Impact of Tumoral β2-Adrenergic Receptor Expression on Chemotherapeutic Response and Prognosis in Patients with Advanced Colorectal Cancer.

Chika Komine, Makoto Sohda, Takehiko Yokobori, Ikuma Shioi, Naoya Ozawa, Yuta Shibasaki, Nobuhiro Nakazawa, Katsuya Osone, Takuya Shiraishi, Takuhisa Okada and 6 more

Abstract read
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Article in Annals of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. 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

16 authors.

Chika KomineDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Makoto SohdaDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan. msohda@gunma-u.ac.jp.
Takehiko YokoboriResearch Program for Omics-Based Medical Science, Division of Integrated Oncology Research, Gunma University Initiative for Advanced Research (GIAR), Maebashi, Gunma, Japan. bori45@gunma-u.ac.jp.
Ikuma ShioiDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Naoya OzawaDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Yuta ShibasakiDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Nobuhiro NakazawaDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Katsuya OsoneDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Takuya ShiraishiDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Takuhisa OkadaDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Akihiko SanoDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Makoto SakaiDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Hiroomi OgawaDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Kyoichi KairaDepartment of Respiratory Medicine, Comprehensive Cancer Center, International Medical Center, Saitama University Hospital, Hidaka, Japan.
Ken ShirabeDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Hiroshi SaekiDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.

Funding

Japanese Society for the Promotion of Science 21K08749Japanese Society for the Promotion of Science 22H02912Japanese Society for the Promotion of Science 22K08766Japanese Society for the Promotion of Science 22K16480Japanese Society for the Promotion of Science 23K15513Japanese Society for the Promotion of Science 23K19496
6 · The paper itself

Abstract

backgroundThe β2-adrenergic receptor (β2-AR) is a therapeutic target for circulatory agonists and exhibits oncogenic activity in several cancers. However, its role in advanced colorectal cancer (CRC) treated using chemotherapy remains unclear. We investigated the potential of β2-AR as a novel chemosensitivity marker and therapeutic target in inoperable CRC.

methodsβ2-AR expression was evaluated immunohistochemically in 80 advanced or recurrent CRC cases for which untreated resected specimens were available before systemic chemotherapy implementation. We assessed the relationship among β2-AR protein expression, clinicopathological factors, therapeutic response, and prognosis. Furthermore, we evaluated the significance of β2-AR as an in vitro and in vivo therapeutic target using CRC cell lines and a CRC xenograft model treated with the β-blocker, propranolol, and other anticancer agents.

resultsHigh tumoral β2-AR expression was associated with shorter progression-free survival and chemotherapeutic resistance in patients treated with oxaliplatin-based regimens and bevacizumab-based regimens. We found no synergistic effect between propranolol and oxaliplatin. However, combined administration of propranolol and bevacizumab induced significant tumor shrinkage in the CRC xenograft model.

conclusionsβ2-AR is a possible biomarker for chemosensitivity and prognosis in advanced CRC. Repositioning existing β-blockers could be beneficial for treating CRC resistant to existing treatment regimens.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorColorectal NeoplasmsDrug Resistance, NeoplasmNeoplasm Recurrence, LocalReceptors, Adrenergic, beta-2AdultAgedAnimalsBevacizumabCell ProliferationFemaleFollow-Up StudiesHumansMaleMiceBevacizumabBiomarkers, TumorOrganoplatinum CompoundsOxaliplatinPropranololReceptors, Adrenergic, beta-2Adrenergic receptorChemosensitivityColon cancerβ-Blocker

Identifiers

What Socratic 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 Socratic graph.