Evidence map›Paper›PMID 26852037›Full record

ArticleGlycoconjugate journal2016

Enzymatic synthesis of lactosylated and sialylated derivatives of epothilone A.

Prakash Parajuli, Ramesh Prasad Pandey, Rit Bahadur Gurung, Ju Yong Shin, Hye Jin Jung, Dae Hee Kim, Jae Kyung Sohng

Abstract read
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Article in Glycoconjugate journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Prakash ParajuliInstitute of Biomolecule Reconstruction, Department of BT-convergent Pharmaceutical Engineering, SunMoon University, 70, Sun Moon-Ro 221, Tangjeonmyun, Asan-Si, Chungnam, 336-708, South Korea.
Ramesh Prasad PandeyInstitute of Biomolecule Reconstruction, Department of BT-convergent Pharmaceutical Engineering, SunMoon University, 70, Sun Moon-Ro 221, Tangjeonmyun, Asan-Si, Chungnam, 336-708, South Korea.
Rit Bahadur GurungInstitute of Biomolecule Reconstruction, Department of BT-convergent Pharmaceutical Engineering, SunMoon University, 70, Sun Moon-Ro 221, Tangjeonmyun, Asan-Si, Chungnam, 336-708, South Korea.
Ju Yong ShinInstitute of Biomolecule Reconstruction, Department of BT-convergent Pharmaceutical Engineering, SunMoon University, 70, Sun Moon-Ro 221, Tangjeonmyun, Asan-Si, Chungnam, 336-708, South Korea.
Hye Jin JungInstitute of Biomolecule Reconstruction, Department of BT-convergent Pharmaceutical Engineering, SunMoon University, 70, Sun Moon-Ro 221, Tangjeonmyun, Asan-Si, Chungnam, 336-708, South Korea.
Dae Hee KimGeneChem, 59-5, Jang-dong, Yuseong-gu, Daejeon, 305-343, South Korea.
Jae Kyung SohngInstitute of Biomolecule Reconstruction, Department of BT-convergent Pharmaceutical Engineering, SunMoon University, 70, Sun Moon-Ro 221, Tangjeonmyun, Asan-Si, Chungnam, 336-708, South Korea. sohng@sunmoon.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epothilone A is a derivative of 16-membered polyketide natural product, which has comparable chemotherapeutic effect like taxol. Introduction of sialic acids to these chemotherapeutic agents could generate interesting therapeutic glycoconjugates with significant effects in clinical studies. Since, most of the organisms biosynthesize sialic acids in their cell surface, they are key mediators in cellular events (cell-cell recognition, cell-matrix interactions). Interaction between such therapeutic sugar parts and cellular polysaccharides could generate interesting result in drugs like epothilone A. Based on this hypothesis, epothilone A glucoside (epothilone A 6-O-β-D-glucoside) was further decorated by conjugating enzymatically galactose followed by sialic acids to generate epothilone A 7-O-β-D-glucopyranosyl, 4'-O-α-D-galactoside i.e., lactosyl epothilone A (lac epoA) and two sialosides of epothilone A namely epothilone A 7-O-β-D-glucopyranosyl, 4'-O-α-D-galactopyranosyl 3″-O-α-N-acetyl neuraminic acid and epothilone A 7-O-β-D-glucopyranosyl, 4'-O-α-D-galactopyranosyl 6″-O-α-N-acetylneuraminic acid i.e., 3'sialyllactosyl epothilone A: 3'SL-epoA, and 6'sialyllactosyl epothilone A: 6'SL-epoA, respectively. These synthesized analogs were spectroscopically analyzed and elucidated, and biologically validated using HUVEC and HCT116 cancer cell lines.

Indexed as

EpothilonesCell Line, TumorHumansHuman Umbilical Vein Endothelial CellsLactic AcidN-Acetylneuraminic Acidepothilone AEpothilonesLactic AcidN-Acetylneuraminic Acid3′Sialyllactosyl epothilone A6′sialyllactosyl epothilone AChemotherapeutic agentEpothilone A 6-O-β-D-glucosideEpothilones

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Registered trials

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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.