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Frontiers in Pharmacology logoLink to Frontiers in Pharmacology
. 2023 Sep 8;14:1274076. doi: 10.3389/fphar.2023.1274076

Corrigendum: Paraptosis: a unique cell death mode for targeting cancer

Sweata Hanson 1,, Aiswarya Dharan 1,, Jinsha P V 1, Sanjay Pal 1, Bipin G Nair 1, Rekha Kar 2, Nandita Mishra 1,*
PMCID: PMC10515721  PMID: 37745056

In the published article, there was an error in Table 3 as published. The cell line type and the signalling pathway and mechanism attributed to the article by Garrido-Armas et al. (2018) was incorrect. The corrected Table 3 appear below.

TABLE 3.

Paraptosis-inducing compounds against cancer cell lines.

Sl. No: Compounds Cell line type Cell line Signalling pathway and mechanism References
1. Breast
i) Curcumin Melanocyte MDA-MB-434S Inhibition of mitochondrial Na+/Ca2+ exchanger (mNCX) and proteasome, pERK1/2↑, p-JNKs↑, Alix↓ Yoon et al. 2010 (2012)
Epithelial MDA-MB-231, HS578T
ii) Dimethoxy curcumin Melanocyte MDA-MB-434S Proteasomal inhibition and ER stress, pERK1/2↑, p-JNKs ↑, Alix↓ Yoon et al. (2014a)
Epithelial MDA-MB-231, HS578T, MCF-7
iii) Celastrol Melanocyte MDA-MB-434S Ca2+ overload, proteasomal inhibition via ER stress, pERK1/2↑, p-JNKs ↑, p-p38 Yoon et al. (2014)
Epithelial MCF-7
iv) 15d-PGJ2 Epithelial MDA-MB-231 Disruption of sulfhydryl homeostasis, ER stress, pERK1/2↑ Kar et al. (2009)
v) Manumycin A Epithelial MDA-MB-231, BT-20 ER stress, accumulation of ubiquitinated proteins, p21↑, p27 ↑, PTEN ↑ Singha et al. (2013)
Lymphoblast HCC1937
vi) Withaferin A Epithelial MDA-MB-231, MCF-7 ER stress, ROS production, Alix↓ Ghosh et al. (2016)
vii) Deoxyelephantopin derivative (DETD) Epithelial MDA-MB-231 Oxidative and ER stress, p-JNK↑ Shiau et al. (2017)
viii) Chalcomoracin Epithelial MDA-MB-231 ROS production, PINK1 ↑, Alix ↓, p-ERK↑ Han et al. (2018)
ix) 6-Shogaol Epithelial MDA-MB-231 Proteasomal inhibition, ER stress Nedungadi, et al. (2018)
x) Plumbagin Epithelial MDA-MB-231 Disruption of sulfhydryl homeostasis and inhibition of proteasome Binoy et al. (2019)
xi) 2′-hydroxy-retrochalcone Epithelial MDA-MB-231 Proteasomal dysfunction and ER stress Nedungadi et al. (2021)
xii) Indirubin-3′-monoxime (I3M) Epithelial MDA-MB-231 Proteasomal dysfunction and ER stress-mediated Ca2+ release. Dilshara et al. (2021)
xiii) Cannabinoids (C6 combination) Epithelial MDA-MB-231, MCF-7 ER stress (GRP78 increase) Schoeman et al. (2020)
xiv) Gambogic Acid Epithelial MDA-MB-453, MDA-MB-468, MDA-MB-435S Disruption of thiol proteostasis Seo et al. (2019)
Melanocyte
xv) 5,7-dibromo-8-(methoxymethoxy)-2-methylquinoline (HQ-11) Epithelial MDA-MB-231, MCF-7 ER stress, proteasomal inhibition, pERK↑ Ma et al. (2022)
xvi) Glabridin Epithelial MDA-MB-231, MCF-7 ER stress, poly ubiquitinated protein accumulation, proteasome suppression, ROS production, MMP loss Cui and Cui (2022)
xvii) Isoxazole derivative of usnic acid Epithelial MDA-MB-231, MCF-7 ER stress, IP3R channel activation Pyrczak-Felczykowska et al. (2022)
xviii) Derivative of pyrazolo[3,4-h]quinoline scaffold (YRL1091) Epithelial MDA-MB-231, MCF-7 ER stress, accumulation of ubiquitinated proteins, ROS production, ERK↑, JNK↑, Alix↓ Nguyen et al. (2022)
xix) Ginger extract Epithelial MDA-MB-231 ER stress, mitochondrial dysfunction, AIF translocation and DNA damage Nedungadi et al. (2021)
xx) Disulfiram oxy-derivatives Epithelial MCF-7 ER stress, mitochondrial damage, 20S proteasome inhibition and actin depolymerization at later stages Solovieva et al. (2022)
2. Brain
i) Curcumin Glioblastoma A172 via microRNAs, AKT-Insulin, and p53-BCL2 networks, and AKT protein level reduction was confirmed Garrido-Armas et al. (2018)
ii) Ophiobolin A Pleomorphicastrocytoid, Neuronal, Fibroblast, Fibroblast) Fibroblast U373-MG, U251N, U251MG, A172 ER stress, NAC inhibition, decrease of BKCa channel Bury et al. (2013)
T98G
iii) Oligomeric Procyanidins Epithelial U-87 Extracellular Ca2+ influx, pERK1/2↑, p-p38 ↑ (Zhang et al., 2010)
iv) Paclitaxel Epithelial U-87 CHX has no effect, MEK, p38 and JNK pathways are not involved Sun et al. (2010)
v) Yessotoxin Muscle cells from intracranial tumor BC3H1 ER and mitochondrial swelling, p-JNK↑ Korsnes et al. (2011)
vi) 1-Desulfo Yessotoxin Muscle cells from intracranial tumor BC3H1 ER and mitochondrial swelling, p-p38↑ Korsnes et al. (2013)
vii) Xanthohumol Epithelial SH-SY5Y ER stress and LC3B upregulation, p38 ↑ Mi et al. (2017)
3. Blood
i) Honokiol Lymphoblast K562 ROS generation ROS generation, ER stress, LC3 upregulation, mTOR and MAPK activated Liu et al. (2021), Wang et al. (2013)
Promyelocyte NB4
ii) Xanthohumol Promyeloblast HL-60 ER stress and LC3B upregulation, p38 ↑ Mi et al. (2017)
iii) Iturin lipopeptide Lymphoblast K562 LC3B and p62 upregulation Zhao et al. (2019)
iv) Brassinin Lymphoblast K562 ROS production, mitochondrial damage, ER stress, and activation of MAPK Yang et al. (2023)
Lymphoblast-like KBM5, LAMA84, and KCL22
4. Cervical
i) Celastrol Epithelial HeLa Proteasome inhibition, Mitochondrial Ca2+ overload, pERK1/2↑, p-JNKs ↑, p-p38 ↑ Wang et al. (2012)
ii) Cyclosporin A Epithelial HeLa, SiHa LC3 upregulation, Cyclophilin B↓, Alix↓ Ram and Ramakrishna (2014)
iii) 8-p-Hydroxybenzoyl tovarol Epithelial HeLa Bip, CHOP, IRE1α and XBP1 upregulation Zhang et al. (2015)
iv) Seleno-DL-Cystine Epithelial HeLa Bip and CHOP polyubiquitination upregulation, ROS generation Wallenberg et al. (2014)
v) Paclitaxel Epithelial HeLa CHX has no effect, MEK, p38 and JNK are not involved Sun et al. (2010)
vi) Wheat germ Agglutinin Epithelial HeLa, SiHa, CaSKi Autophagy-linked FYVE (Alfy) protein inhibition, ER stress, LC3B upregulation Tsai et al. (2017)
vii) 2′-hydroxy-retrochalcone Epithelial HeLa Proteasomal dysfunction, ER stress, LC3 upregulation Nedungadi et al. (2021)
5. Thyroid
i) Tunicamycin Epithelial 8505C, CAL62, FRO cell lines Bip, CHOP, p-PERK and IRE1 upregulation Kim et al. (2014)
6. Liver
i) Hesperidin Epithelial HepG2 Mitochondrial dysfunction and Ca2+ overload, p-ERK↑ Yumnam et al., 2016)
ii) Cis-Nerolidol Epithelial HepG2/C3 A ER stress, increased activity of cytochrome P450 enzymes Biazi et al. (2017)
iii) Gambogic Acid Epithelial; diffusely spreading cells SNU-449 Proteasomal inhibition and ER stress, ROS independent- mitochondrial depolarization Seo et al. (2019)
7. Colon
i) Curcumin Epithelial HCT116 Proteasome inhibition ROS, Mitochondrial Ca2+ overload, LC3 upregulation, pERK1/2↑, p-JNKs↑, Alix↓ Lee et al. (2015)
ii) Celastrol Epithelial DLD-1, RKO Proteasome inhibition, Mitochondrial Ca2+ overload, pERK1/2↑, p-JNKs ↑, p-p38 ↑ Yoon et al. (2014)
iii) 15d-PGJ2 Epithelial HCT116 Disruption of sulfhydryl homeostasis LC3 upregulation, pERK1/2↑ Kar et al. (2009)
iv) Ginsenoside Rh2 Epithelial HCT116, SW480 p53 activation, activation of death by antioxidants Li et al. (2011), Wan et al. (2018)
v) Protopanaxadiol Epithelial HCT116, SW480 Death acceleration by inhibiting ROS generation, NF-κB activated Wang et al. (2013)
vi) ɣ-Tocotrienol Epithelial SW620 and HCT-8 Wnt signals↓ (β-catenin, cyclin D, c-Jun) Zhang et al. (2011) (2013)
δ-Tocotrienol Epithelial SW620 Wnt signals↓ (β-catenin, cyclin D, c-Jun)
vii) Iturin A-like lipopeptides Epithelial Caco-2 ER stress, ROS generation, Ca2+ Zhao et al. (2019)
viii) Loperamide Epithelial DLD-1, SW-480, SW-620, HCT116 ER stress, Ca2+ imbalance and CHOP↑ Kim et al. (2019)
ix) Purified resin glycoside fraction (Pharbitidis Semen) Epithelial HT-29 and HCT-116 Chloride intracellular channel-1 activation and intracellular Cl↑, MAPK activation Zhu et al. (2019)
8. Prostate
i) Curcumin Epithelial PC-3M Proteasome inhibition ROS, Mitochondrial Ca2+ overload, LC3 upregulation, pERK1/2↑, p-JNKs↑, Alix↓ Lee et al. (2015)
ii) 15d-PGJ2 Epithelial DU145 Disruption of sulfhydryl homeostasis LC3 upregulation, pERK1/2↑ Kar et al. (2009)
iii) Benzo[a]quinolizidine analogs Epithelial PC3 ER stress and LC3B upregulation Zheng et al. 2016)
iv) Chalcomoracin Epithelial LNCaP, PC-3 ROS generation, ER stress, PINK1 ↑, Alix ↓, p-ERK↑ Han et al, 2018)
v) δ-Tocotrienol Epithelial CRPC cells—DU145, PC-3 ER stress, LC3 and p62 upregulation, p-JNK ↑, p-p38 ↑ Fontana et al. (2020)
9. Ovarian
i) Morusin Epithelial A2780, HO-8910, SKOV3 Ca2+ overload, ROS generation and loss of mitochondrial membrane potential Xue et al. (2018)
ii) Elaiophylin Epithelial SKOV3, OVCAR8, UWB1.289, SW626 ER stress, SHP2/SOS1/MAPK↑ Li et al. (2022)
10. Lung
(i) Cyclosporin A Epithelial A549 LC3 upregulation, Cyclophilin B↓, Alix↓ Ram and Ramakrishna (2014)
ii) Paclitaxel Epithelial A549 CHX has no effect, MEK, p38 and JNK are not involved Guo et al. (2010)
Epithelial ASTC-a-1
iii) 6-Shogaol Epithelial A549 Proteasome inhibition, ER stress, ROS generation, LC3 upregulation Nedungadi et al. (2018)
iv) Hinokitiol copper complex Epithelial A549 Proteasome inhibition, ER stress Chen et al. (2017)
v) Chalcomoracin Epithelial H460 ER stress, MAPK activation Han et al. (2018)
Epithelial A549
Adenocyte PC-9
vi) Paris Saponin II (PSII) Epithelial NCI-H460 ER stress, JNK pathway activation Man et al. (2020)
Epithelial NCI-H520
vii) Prenylated bibenzyls (Radula constricta) Epithelial A549, NCI-H1299 ROS elevation and loss in mitochondrial membrane potential Zhang et al. (2019)
viii) Gambogic Acid Epithelial NCI-H460 Proteasomal inhibition and ER stress, ROS independent- mitochondrial depolarization Seo et al. (2019)
ix) Epimedokoreanin B Epithelial A549, NCL-H292 ER stress, autophagosome accumulation, ROS production, loss of MMP, UPR signaling Zheng et al. (2022)
x) DHW-221 Epithelial A549 ER stress, PI3K/mTOR inhibition, MAPK activation Liu et al. (2022)
xi) Ginger extract Epithelial A549 ER stress, mitochondrial dysfunction, AIF translocation and DNA damage Nedungadi et al. (2021)
11. Skin
i) Cyclosporin A Keratinocyte HaCaT LC3 upregulation, Cyclophilin B↓, Alix↓ (Ram and Ramakrishna (2014)
ii) δ-tocotrienol Epithelial A375 Ca2+ overload and ROS generation, MAPK activation Raimondi et al. (2021)
12. Bone
i) Cyclosporin A Epithelial U2OS, Saos-2 LC3 upregulation, Cyclophilin B↓, Alix↓ Ram and Ramakrishna (2014)
13. Kidney and Bladder
i) Jolkinolide B Epithelial T24, UM-UC-3, T24/CDDP ROS-mediated ER stress, MAPK and ERK activation Sang et al. (2021)
14. Oral
i) Isorhamnetin (3′-Methoxy-3,4′,5,7-tetrahydroxyflavone) Epithelial HSC-3, HSC-4, PE/CA-PJ15 ↑ROS generation, ERK/MAPK Chen et al. (2021)
15. Pancreas
i) Gambogic Acid Epithelial BxPC-3 Proteasomal inhibition and ER stress, ROS- independent mitochondrial depolarization Seo et al. (2019)
16. Stomach
i) Gambogic Acid Epithelial SNU-668 (gastric cancer) Proteasomal inhibition and ER stress, ROS independent- mitochondrial depolarization Seo et al. 2019)

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

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