Evidence map›Paper›PMID 38905027›Full record

ReviewBreast disease2024

Lectins as a promising therapeutic agent for breast cancer: A review.

Keerti Singh, Lokita Agrawal, Rhea Gupta, Divyam Singh, Meghavi Kathpalia, Navkiran Kaur

Abstract readReview
In one paragraph

Review in Breast disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Expression of 9-Life (Basel, Switzerland) · 2025
    Article
  7. 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

6 authors.

Keerti SinghAmity Institute of Biotechnology, Amity University, Noida, Uttar Pradesh, India.
Lokita AgrawalAmity Institute of Biotechnology, Amity University, Noida, Uttar Pradesh, India.
Rhea GuptaAmity Institute of Biotechnology, Amity University, Noida, Uttar Pradesh, India.
Divyam SinghAmity Institute of Biotechnology, Amity University, Noida, Uttar Pradesh, India.
Meghavi KathpaliaAmity Institute of Biotechnology, Amity University, Noida, Uttar Pradesh, India.
Navkiran KaurAmity Institute of Biotechnology, Amity University, Noida, Uttar Pradesh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficient treatment of cancer has been a subject of research by scientists for many years. Current treatments for cancer, such as radiotherapy, chemotherapy and surgery have been used in traditional combination therapy, but they have major setbacks like non-specificity, non-responsiveness in certain cancer types towards treatment, tumor recurrence, etc. Epidemiological data has shown that breast cancer accounts for 14% of cancer cases occurring in Indian women. In recent years, scientists have started to focus on the use of natural compounds like lectins obtained from various sources to counter the side effects of traditional therapy. Lectins like Sambucus nigra Agglutinin, Maackia amurensis lectin, Okra lectins, Haliclona caerulea lectin, Sclerotium rolfsii lectin, etc., have been discovered to have both diagnostic and therapeutic potential for breast cancer patients. Lectins have been found to have inhibitory effects on various cancer cell activities such as neo-angiogenesis, causing cell cycle arrest at the G1 phase, and inducing apoptosis. The major idea behind the use of lectins in cancer diagnostics and therapeutics is their capability to bind to glycosylated proteins that are expressed on the cell surface. This review focuses on an exploration of the roles of post-translational modification in cancer cells, especially glycosylation, and the potential of lectins in cancer diagnosis and therapeutics.

Indexed as

Breast NeoplasmsLectinsAntineoplastic AgentsApoptosisFemaleGlycosylationHumansProtein Processing, Post-TranslationalAntineoplastic AgentsLectinsapoptosisCancercell cyclechemotherapyG1 phaseglycosylated proteinsHaliclona caerulea lectinlectinsMaackia amurensis lectinno-angiogenesisOkra lectinspost-translational modificationradiotherapySambucus nigra AgglutininSclerotium rolfsii lectinsurgery

Identifiers

PMID38905027
PMCPMC11307042

What OpenQuestion holds

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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 OpenQuestion graph.