Evidence map›Paper›PMID 29083380›Full record

ReviewMedical sciences (Basel, Switzerland)2016

Combination of mTOR and MAPK Inhibitors-A Potential Way to Treat Renal Cell Carcinoma.

Ashutosh Chauhan, Deepak Kumar Semwal, Satyendra Prasad Mishra, Sandeep Goyal, Rajendra Marathe, Ruchi Badoni Semwal

Open access · goldAbstract readReview
In one paragraph

Review in Medical sciences (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 14 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

6 authors at 3 institutions in 2 countries.

Ashutosh ChauhanDepartment of Urology, Postgraduate Institute of Medical Education & Research, Chandigarh 160012, India. ashutosh_biotech2006@yahoo.com.
Deepak Kumar SemwalDepartment of Phytochemistry, Faculty of Biomedical Sciences, Uttarakhand Ayurved University, Harrawala, Dehradun 248001, Uttarakhand, India. dr_dks.1983@yahoo.co.in.
Satyendra Prasad MishraVice Chancellor, Uttarakhand Ayurved University, Harrawala, Dehradun 248001, Uttarakhand, India. vc@uau.ac.in.
Sandeep GoyalDepartment of Hepatology, Postgraduate Institute of Medical Education & Research, Chandigarh 160012, India. sandeepgoyalpgi@gmail.com.
Rajendra MaratheDepartment of Pediatrics, Postgraduate Institute of Medical Education & Research, Chandigarh 160012, India. rajendra.bt09@gmail.com.
Ruchi Badoni SemwalDepartment of Pharmaceutical Sciences, Tshwane University of Technology, Pretoria 0001, South Africa. semwalrb@tut.ac.za.
Post Graduate Institute of Medical Education and Research · INUttarakhand Ayurved University · INTshwane University of Technology · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma (RCC) is the most common neoplasm that occurs in the kidney and is marked by a unique biology, with a long history of poor response to conventional cancer treatments. In the past few years, there have been significant advancements to understand the biology of RCC. This has led to the introduction of novel targeted therapies in the management of patients with metastatic disease. Patients treated with targeted therapies for RCC had shown positive impact on overall survival, however, no cure is possible and patients need to undergo treatment for long periods of time, which raises challenges to manage the associated adverse events. Moreover, many patients may not respond to it and even response may not last long enough in the responders. Many inhibitors of the Mammalian target of Rapamycin (mTOR) signaling pathway are currently being used in treatment of advanced RCC. Studies showed that inhibitions of mTOR pathways induce Mitogen-Activated Protein Kinase (MAPK) escape cell death and cells become resistant to mTOR inhibitors. Because of this, there is a need to inhibit both pathways with their inhibitors comparatively for a better outcome and treatment of patients with RCC.

Indexed as

mammalian target of rapamycinmitogen activated protein kinaserenal cell carcinomatarget therapy

Identifiers

PMID29083380
PMCPMC5635794
OpenAlexW2536795512

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.