Evidence map›Paper›PMID 31439015›Full record

ReviewJournal of experimental & clinical cancer research : CR2019

Cancer therapeutics using survivin BIRC5 as a target: what can we do after over two decades of study?

Fengzhi Li, Ieman Aljahdali, Xiang Ling

Open access · goldAbstract readReview
In one paragraph

Review in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 147 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
147citing papers in PubMed, 1 pooled it
11.6field-weighted citation impact, top 1% 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

147 citing papers in PubMed, 1 synthesis or guideline pooled it, 262 citations in OpenAlex.

  1. Pooled it
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  8. Novel quinoxaline-based survivin degraders overcome docetaxel-resistance in castration-resistant prostate cancer.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2026
    Review
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  12. International journal of nanomedicine · 2026
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87 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Fengzhi LiDepartment of Pharmacology & Therapeutics, Roswell Park Comprehensive Cancer Center, Elm and Carlton Streets, Buffalo, New York, 14263, USA. fengzhi.li@roswellpark.org.ORCID http://orcid.org/0000-0002-2299-7951
Ieman AljahdaliDepartment of Pharmacology & Therapeutics, Roswell Park Comprehensive Cancer Center, Elm and Carlton Streets, Buffalo, New York, 14263, USA.
Xiang LingDepartment of Pharmacology & Therapeutics, Roswell Park Comprehensive Cancer Center, Elm and Carlton Streets, Buffalo, New York, 14263, USA.
Roswell Park Comprehensive Cancer Center · US

Funding

A small molecule broad spectrum inhibitor of antiapoptotic genes to treat cancerR44CA176937 · NCI · CANGET BIOTEKPHARMA, LLC · PI LI, FENGZHI, LING, XIANG · 2014 to 2018
$2.3M
A novel small molecule FL7N-1 for treating pediatric cancer retinoblastomaR43CA221389 · NCI · CANGET BIOTEKPHARMA, LLC · PI LI, FENGZHI, LING, XIANG · 2018 to 2018
$225k
NCI NIH HHS R43 CA221389NCI NIH HHS R44 CA176937NIH/NCI R43CA221389NIH/NCI R44CA176937
6 · The paper itself

Abstract

Survivin (also named BIRC5) is a well-known cancer therapeutic target. Since its discovery more than two decades ago, the use of survivin as a target for cancer therapeutics has remained a central goal of survivin studies in the cancer field. Many studies have provided intriguing insight into survivin's functional role in cancers, thus providing promise for survivin as a cancer therapeutic target. Despite this, moving survivin-targeting agents into and through the clinic remains a challenge. In order to address this challenge, we may need to rethink current strategies in order to develop a new mindset for targeting survivin. In this Review, we will first summarize the current survivin mechanistic studies, and then review the status of survivin cancer therapeutics, which is classified into five categories: (i) survivin-partner protein interaction inhibitors, (ii) survivin homodimerization inhibitors, (iii) survivin gene transcription inhibitors, (iv) survivin mRNA inhibitors and (v) survivin immunotherapy. We will then provide our opinions on cancer therapeutics using survivin as a target, with the goal of stimulating discussion that might facilitate translational research for discovering improved strategies and/or more effective anticancer agents that target survivin for cancer therapy.

Indexed as

Molecular Targeted TherapyAntineoplastic AgentsHumansNeoplasmsPrognosisSurvivinAntineoplastic AgentsBIRC5 protein, humanSurvivinBIRC5cIAP2FL118Mcl-1MdmXsurvivinSurvivin cancer therapeuticssurvivin immunotherapyXIAPYM155

Identifiers

PMID31439015
PMCPMC6704566
OpenAlexW2969272216

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.