# Novel harmine derivatives for tumor targeted therapy

**Authors:** Siwen Li, Aqin Wang, Fan Gu, Zhaohui Wang, Caiping Tian, Zhiyu Qian, Liping Tang, Yueqing Gu

PMC · DOI: 10.18632/oncotarget.3276 · 2015-04-22

## TL;DR

Researchers developed new versions of a plant compound called harmine to make it more effective and less toxic for cancer treatment.

## Contribution

The study introduces two novel harmine derivatives with improved therapeutic efficacy and reduced toxicity for targeted cancer therapy.

## Key findings

- Modified harmine derivatives 2DG-Har-01 and MET-Har-02 showed higher therapeutic effects than unmodified harmine.
- MET-Har-02 was more potent than 2DG-Har-01 in preclinical tests.
- The derivatives demonstrated potential for targeted cancer therapy with reduced systemic toxicity.

## Abstract

Harmine is a beta-carboline alkaloid found in medicinal plant PeganumHarmala, which has served as a folk anticancer medicine. However, clinical applications of harmine were limited by its low pharmacological effects and noticeable neurotoxicity. In this study, we modified harmine to increase the therapeutic efficacy and to decrease the systemic toxicity. Specifically, two tumor targeting harmine derivatives 2DG-Har-01 and MET-Har-02 were synthesized by modifying substituent in position-2, -7 and -9 of harmine ring with two different targeting group2-amino-2-deoxy-D-glucose (2DG) and Methionine (Met), respectively. Their therapeutic efficacy and toxicity were investigated both in vitro and in vivo. Results suggested that the two newharmine derivatives displayed much higher therapeutic effects than non-modified harmine. In particular, MET-Har-02 was more potent than 2DG-Har-01 with promising potential for targeted cancer therapy.

## Linked entities

- **Chemicals:** harmine (PubChem CID 5280953), 2DG (PubChem CID 40), Methionine (PubChem CID 876)
- **Diseases:** cancer (MONDO:0004992)
- **Species:** Peganum harmala (taxon 43879)

## Full-text entities

- **Genes:** Casp9 (caspase 9) [NCBI Gene 12371] {aka APAF-3, CASP-9, Caspase-9, ICE-LAP6, Mch6}, LAT2 (linker for activation of T cells family member 2) [NCBI Gene 7462] {aka HSPC046, LAB, NTAL, WBSCR15, WBSCR5, WSCR5}, Slc2a1 (solute carrier family 2 (facilitated glucose transporter), member 1) [NCBI Gene 20525] {aka GT1, Glut-1, Glut1, M100200, Rgsc200}, ANXA5 (annexin A5) [NCBI Gene 308] {aka ANX5, CPB-I, ENX2, HEL-S-7, PP4, RPRGL3}, Casp8 (caspase 8) [NCBI Gene 12370] {aka CASP-8, FLICE, MACH, Mch5}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, SLC7A5 (solute carrier family 7 member 5) [NCBI Gene 8140] {aka 4F2LC, CD98, D16S469E, E16, LAT1, MPE16}, Slc17a5 (solute carrier family 17 (anion/sugar transporter), member 5) [NCBI Gene 235504] {aka 4631416G20Rik, 4732491M05, AST, ISSD, NSD, SD}, Gpt (glutamic pyruvic transaminase, soluble) [NCBI Gene 76282] {aka 1300007J06Rik, 2310022B03Rik, ALT, ALT1, Gpt-1, Gpt1}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, Bcl2l1 (BCL2-like 1) [NCBI Gene 12048] {aka Bcl(X)L, Bcl-XL, Bcl2l, BclX, bcl-x, bcl2-L-1}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}
- **Diseases:** neural and systemic (MESH:C536149), pathological damage (MESH:D005598), Acute toxicities (MESH:D000208), death (MESH:D003643), cytotoxic (MESH:D064420), hepatocellular carcinoma (MESH:D006528), 2DG- (MESH:D018149), lung cancer (MESH:D008175), tumor metastasis (MESH:D009362), pancreatic cancer (MESH:D010190), liver (MESH:D017093), Ehrlich solid carcinoma (MESH:D002286), cell (MESH:D002292), supination (MESH:D020425), Tetanus (MESH:D013746), breast cancer (MESH:D001943), liver toxicity (MESH:D056486), tremor (MESH:D014202), abnormal behaviors (MESH:D001523), Necrotic (MESH:D009336), Neurotoxic (MESH:D020258), Tumor (MESH:D009369), hepatic edema (MESH:D004487),  (MESH:D010523)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Peganum harmala (species) [taxon 43879], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Met in position-7
- **Cell lines:** A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), L-02 — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_6926), S180 — Mus musculus (Mouse), Mouse fibrosarcoma, Cancer cell line (CVCL_2874), LOVO — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0399), PC12 — Rattus norvegicus (Rat), Rat adrenal gland pheochromocytoma, Cancer cell line (CVCL_0481), MCF-7 — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_0031), SMMC-7721 — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0534), S180 sarcoma — Mus musculus (Mouse), Mouse fibrosarcoma, Cancer cell line (CVCL_3598), MET- — Homo sapiens (Human), Skin squamous cell carcinoma, Cancer cell line (CVCL_LN09), HuH7 — Homo sapiens (Human), Adult hepatocellular carcinoma, Cancer cell line (CVCL_0336), PC-3 — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_0035), HepG-2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4496197/full.md

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Source: https://tomesphere.com/paper/PMC4496197