Evidence map›Paper›PMID 37997805›Full record

ReviewEndocrine, metabolic & immune disorders drug targets2024

Study Deciphering the Crucial Involvement of Notch Signaling Pathway in Human Cancers.

Pratibha Pandey, Fahad Khan, Megha Singh, Aditi Verma, Hariom Kumar, Avijit Mazumder, Gurmeen Rakhra

Abstract readReview
PubMed Publisher
In one paragraph

Review in Endocrine, metabolic & immune disorders drug targets, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
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

7 authors at 2 institutions in 1 country.

Pratibha PandeyDepartment of Biotechnology, Noida Institute of Engineering and Technology, Greater Noida, UP, India.
Fahad KhanDepartment of Biotechnology, Noida Institute of Engineering and Technology, Greater Noida, UP, India.
Megha SinghDepartment of Biotechnology, Noida Institute of Engineering and Technology, Greater Noida, UP, India.
Aditi VermaDepartment of Biotechnology, Noida Institute of Engineering and Technology, Greater Noida, UP, India.
Hariom KumarDepartment of Biotechnology, Noida Institute of Engineering and Technology, Greater Noida, UP, India.
Avijit MazumderDepartment of Pharmacology, Noida Institute of Engineering and Technology (Pharmacy Institute), Greater Noida, 201306, India.
Gurmeen RakhraDepartment of Biochemistry, Lovely Professional University, Phagwara, Punjab, India.
Jaypee Institute of Information Technology · INLovely Professional University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, dysregulation of the notch pathway has been associated with the development and progression of various cancers. Notch signaling is involved in several cellular processes, such as proliferation, differentiation, apoptosis, and angiogenesis, and its abnormal activation can lead to uncontrolled cell growth and tumorigenesis. In various human cancers, the Notch pathway has been shown to have both tumor-promoting and tumor-suppressive effects, depending on the context and stage of cancer development. Notch signaling has been implicated in tumor initiation, cancer cell proliferation, cell migration and maintenance of cancer stem cells in several human cancers, including leukemia, breast, pancreatic and lung cancer. Understanding the role of the Notch pathway in cancer development and progression may provide new opportunities for the development of potent targeted therapies for cancer treatment. Several drugs targeting the Notch pathway are currently in preclinical or clinical development and may hold promise for anticancer therapy in the future.

Indexed as

NeoplasmsReceptors, NotchSignal TransductionAnimalsAntineoplastic AgentsCell ProliferationHumansMolecular Targeted TherapyNeoplastic Stem CellsAntineoplastic AgentsReceptors, Notchapoptosiscancerdrug targetingNotchsignaling pathwaytumor.

Identifiers

PMID37997805
OpenAlexW4388982442

What OpenQuestion 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 OpenQuestion graph.