Evidence map›Paper›PMID 36142303›Full record

ArticleInternational journal of molecular sciences2022

Potential Therapeutic Agents against Paclitaxel-And Sorafenib-Resistant Papillary Thyroid Carcinoma.

Seok-Mo Kim, Keunwan Park, Jin Hong Lim, Hyeok Jun Yun, Sang Yong Kim, Kyung Hwa Choi, Chan Wung Kim, Jae Ha Lee, Raymond Weicker, Cheol-Ho Pan and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 16% of its field
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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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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

11 authors at 2 institutions in 1 country.

Seok-Mo KimDepartment of Surgery, Thyroid Cancer Center, Gangnam Severance Hospital, Institute of Refractory Thyroid Cancer, Yonsei University College of Medicine, Seoul 06273, Korea.ORCID 0000-0001-8070-0573
Keunwan ParkNatural Product Informatics Research Center, KIST Gangneung Institute of Natural Products, Gangneung 25451, Korea.ORCID 0000-0002-8783-9495
Jin Hong LimDepartment of Surgery, Gangnam Severance Hospital, Yonsei University College of Medicine, 211 Eonjuro, Gangnam-gu, Seoul 06273, Korea.ORCID 0000-0002-1970-8223
Hyeok Jun YunDepartment of Surgery, Thyroid Cancer Center, Gangnam Severance Hospital, Institute of Refractory Thyroid Cancer, Yonsei University College of Medicine, Seoul 06273, Korea.ORCID 0000-0001-6004-0782
Sang Yong KimDepartment of Surgery, Yonsei University College of Medicine, 50-1, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea.
Kyung Hwa ChoiDepartment of Urology, CHA Bundang Medical Center, CHA University, Seongnam 13496, Korea.
Chan Wung KimCKP Therapeutics, Inc., 110 Canal Street, 4th Floor, Lowell, MA 01852, USA.
Jae Ha LeeCKP Therapeutics, Inc., 110 Canal Street, 4th Floor, Lowell, MA 01852, USA.
Raymond WeickerCKP Therapeutics, Inc., 110 Canal Street, 4th Floor, Lowell, MA 01852, USA.
Cheol-Ho PanNatural Product Informatics Research Center, KIST Gangneung Institute of Natural Products, Gangneung 25451, Korea.ORCID 0000-0002-0322-8030
Ki Cheong ParkDepartment of Surgery, Yonsei University College of Medicine, 50-1, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea.ORCID 0000-0002-3435-3985
Yonsei University · KRCHA University Bundang Medical Center · KR

Funding

Korea Health Industry Development Institute HI18C1188the National Research Foundation of Korea NRF-2017R1D1A1B03029716
6 · The paper itself

Abstract

Thyroid carcinoma, a disease in which malignant cells form in the thyroid tissue, is the most common endocrine carcinoma, with papillary thyroid carcinoma (PTC) accounting for nearly 80% of total thyroid carcinoma cases. However, the management of metastatic or recurrent therapy-refractory PTC is challenging and requires complex carcinoma therapy. In this study, we proposed a new clinical approach for the treatment of therapy-refractory PTC. We identified sarco/endoplasmic reticulum calcium ATPase (SERCA) as an essential factor for the survival of PTC cells refractory to the treatment with paclitaxel or sorafenib. We validated its use as a potential target for developing drugs against resistant PTC, by using patient-derived paclitaxel- or sorafenib-resistant PTC cells. We further discovered novel SERCA inhibitors, candidates 7 and 13, using the evolutionary chemical binding similarity method. These novel SERCA inhibitors determined a substantial reduction of tumors in a patient-derived xenograft tumor model developed using paclitaxel- or sorafenib-resistant PTC cells. These results could provide a basis for clinically meaningful progress in the treatment of refractory PTC by identifying a novel therapeutic strategy: using a combination therapy between sorafenib or paclitaxel and specific SERCA inhibitors for effectively and selectively targeting extremely malignant cells such as antineoplastic-resistant and carcinoma stem-like cells.

Indexed as

Antineoplastic AgentsThyroid NeoplasmsHumansNeoplasm Recurrence, LocalPaclitaxelPhenylurea CompoundsSorafenibThyroid Cancer, PapillaryAntineoplastic AgentsPaclitaxelPhenylurea CompoundsSorafenibdrug-resistant papillary thyroid carcinomapaclitaxelpatient-derived xenograft tumor modelsorafenib

Identifiers

PMID36142303
PMCPMC9499486
OpenAlexW4296137186

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.