# Development of a Mechanism of Action-Reflective Cell-Based Reporter Gene Assay for Measuring Bioactivities of Therapeutic Glucagon-like Peptide-2 Analogues

**Authors:** Xiaoming Zhang, Chunyan Li, Zhe Deng, Chenggang Liang, Jing Li

PMC · DOI: 10.3390/molecules30091915 · Molecules · 2025-04-25

## TL;DR

Researchers developed a cell-based test to measure the effectiveness of GLP-2 analogues, which are promising treatments for intestinal and bone diseases.

## Contribution

A new cell-based reporter gene assay was created to accurately assess the bioactivity of GLP-2 analogues.

## Key findings

- The assay showed good accuracy, linearity, precision, and specificity for measuring GLP-2 analogue potency.
- RNA sequencing revealed that GLP-2 analogues have multi-target regulatory effects.
- The assay can be used for stability testing, drug screening, and therapeutic monitoring of GLP-2 analogues.

## Abstract

Glucagon-like peptide-2 (GLP-2) is a gut hormone that plays a pivotal role in regulating intestinal epithelial cell growth and function, making it a promising therapeutic agent for intestinal damage and bone-related diseases. Nonetheless, the therapeutic potential of GLP-2 is substantially diminished due to its inactivation by dipeptidyl peptidase 4 (DPP-4). In recent years, advancements have been made in developing dipeptidyl peptidase 4 (DPP-4) resistant GLP-2 analogues with an extended half-life. The murine model with extensive experimental bowel resection maintained on parenteral nutrition has been used for assessing the physiology and pharmacology of GLP-2, and for the preclinical validation of GLP-2 analogues. However, it possesses certain limitations, such as complex procedure, considerable variability, and time-consuming nature. Consequently, there is a pressing need for the development of a cell-based bioassay to assess GLP-2 analogues. Here, we successfully developed a mechanism-of-action (MOA)-reflective cell-based reporter gene assay (RGA), utilizing a stable HEK293 cell line expressing the GLP-2 receptor and a luciferase reporter gene. This innovative approach allows for precise quantification of the potency of GLP-2 analogues. The RGA demonstrated good accuracy, linearity, precision, and specificity, with potential applications in stability testing, drug screening, and therapeutic monitoring of GLP-2 analogues. Moreover, RNA sequencing reveals the multi-target regulatory effect of GLP-2 analogues. The establishment of this RGA provides a valuable tool for evaluating the potency of GLP-2 analogues and the screening of potential therapeutic drugs targeting to GLP-2 receptor.

## Linked entities

- **Proteins:** GCG (glucagon), DPP4 (dipeptidyl peptidase 4), LOC113215983 (luciferin 4-monooxygenase-like)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** GLP2R (glucagon like peptide 2 receptor) [NCBI Gene 9340], GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}
- **Diseases:** intestinal damage (MESH:D007410), bone-related diseases (MESH:D001847)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** HEK293 — Homo sapiens (Human), Transformed cell line (CVCL_0045)

## Full text

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## Figures

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## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12073449/full.md

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Source: https://tomesphere.com/paper/PMC12073449