Evidence map›Paper›PMID 36238133›Full record

ArticleOncoTargets and therapy2022

Upregulated Ubiquitin D is a Favorable Prognostic Indicator for Rectal Cancer Patients Undergoing Preoperative Concurrent Chemoradiotherapy.

Chia-Lin Chou, Tzu-Ju Chen, Wan-Shan Li, Sung-Wei Lee, Ching-Chieh Yang, Yu-Feng Tian, Cheng-Yi Lin, Hong-Lin He, Hung-Chang Wu, Yow-Ling Shiue and 2 more

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

12 authors at 6 institutions in 1 country.

Chia-Lin ChouDepartment of Medical Technology, Chung Hwa University of Medical Technology, Tainan, 717, Taiwan.
Tzu-Ju ChenDepartment of Medical Technology, Chung Hwa University of Medical Technology, Tainan, 717, Taiwan.
Wan-Shan LiDepartment of Medical Technology, Chung Hwa University of Medical Technology, Tainan, 717, Taiwan.
Sung-Wei LeeDepartment of Radiation Oncology, Chi Mei Medical Center, Liouying, 736, Taiwan.
Ching-Chieh YangDepartment of Radiation Oncology, Chi Mei Medical Center, Tainan, 710, Taiwan.
Yu-Feng TianDivision of Colon and Rectal Surgery, Department of Surgery, Chi Mei Medical Center, Tainan, 710, Taiwan.
Cheng-Yi LinDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Chi Mei Medical Center, Tainan, 710, Taiwan.
Hong-Lin HeDepartment of Pathology, E-DA Hospital & E-DA Cancer Hospital, I-Shou University, Kaohsiung, 82445, Taiwan.
Hung-Chang WuCollege of Pharmacy and Science, Chia Nan University, Tainan, Taiwan.
Yow-Ling ShiueInstitute of Biomedical Science, National Sun Yat-Sen University, Kaohsiung, 804, Taiwan.
Chien-Feng LiInstitute of Precision Medicine, National Sun Yat-Sen University, Kaohsiung, 804, Taiwan.
Yu-Hsuan KuoInstitute of Biomedical Science, National Sun Yat-Sen University, Kaohsiung, 804, Taiwan.
Chia Nan University of Pharmacy and Science · TWChi Mei Medical Center · TWChung Hwa University of Medical Technology · TWI-Shou University · TWNational Health Research Institutes · TWNational Sun Yat-sen University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: For locally advanced rectal cancer, neoadjuvant concurrent chemoradiotherapy (CCRT) allows tumor downstaging and makes curative radical proctectomy possible. However, we lack a genetic biomarker to predict cancer prognosis or treatment response. We investigated the association between ubiquitin D (UBD) expression and clinical outcomes in rectal cancer patients receiving CCRT. Patients and Methods: We analyzed the genes associated with the protein modification process (GO:0036211) and identified the UBD gene as the most relevant among the top 7 differentially expressed genes associated with CCRT resistance. We collected tissue specimens from 172 rectal cancer patients who had received CCRT followed by a curative proctectomy. We examine the relationship between UBD expression and patient characteristics, pathological findings, and patient survival, such as metastasis-free survival (MeFS) and disease-specific survival. Results: Upregulated UBD expression was associated with lower pre-CCRT tumor T stage (P = 0.009), lower post-CCRT tumor T stage (P < 0.001), lower post-CCRT nodal stage (P < 0.001), less vascular invasion (P = 0.015), and better tumor regression (P < 0.001). Using univariate analysis, we found that high UBD expression was correlated with better disease-free survival (DFS) (P < 0.0001), local recurrence-free survival (LRFS) (P < 0.0001) and MeFS (P < 0.0001). Moreover, multivariate analysis demonstrated that high UBD expression was associated with superior DFS (P < 0.001), LRFS (P = 0.01), and MeFS (P = 0.004). Conclusion: UBD upregulation was linked to better clinical prognosis, favorable pathological features, and good treatment response in rectal cancer patients undergoing CCRT. These results suggest UBD is a biomarker for rectal cancer.

Indexed as

concurrent chemoradiotherapyFAT10rectal cancerUBDubiquitin D

Identifiers

PMID36238133
PMCPMC9553428
OpenAlexW4304151166

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.