Evidence map›Paper›PMID 39548458›Full record

ArticleBMC cancer2024

Exploring the correlation between Tom1L1 and the efficacy of neoadjuvant chemotherapy for locally progressive mid-low rectal cancer.

Meng Li, Zeyu Li, Xueliang Wu, Yubo Pan, Likun Wang, Jun Xue, Tian Li

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Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Meng Li *Department of General Surgery, The First Affiliated Hospital of Hebei North University, 12 Changqing Rd, Zhangjiakou, 075000, China.
Zeyu Li *Jinfeng Laboratory, Chongqing, 401329, China.
Xueliang WuDepartment of General Surgery, The First Affiliated Hospital of Hebei North University, 12 Changqing Rd, Zhangjiakou, 075000, China. wxlwlk@163.com.
Yubo Pan *Department of Orthopedics, Third Affiliated Hospital of Naval Medical University, Shanghai, 200438, China.
Likun WangDepartment of Ultrasound Medicine, The First Affiliated Hospital of Hebei North University, Zhangjiakou, 075000, China. wanglikun@tmu.edu.cn.
Jun XueDepartment of General Surgery, The First Affiliated Hospital of Hebei North University, 12 Changqing Rd, Zhangjiakou, 075000, China. yfyxuejun@163.com.
Tian LiSchool of Basic Medicine, Fourth Military Medical University, Xi'an, 710032, China. fmmult@foxmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the specificity of Target of Myb1-Like1 (Tom1L1) expression in colorectal adenocarcinoma tissues and analyze the predictive value of Tom1L1 in the efficacy of neoadjuvant chemotherapy for patients with rectal adenocarcinoma.

methodsThe cancerous tissues and paracancerous normal tissues of 102 patients diagnosed with colorectal adenocarcinoma without treatment were selected; quantitative polymerase chain reaction (qPCR), Western blot and immunohistochemistry (IHC) were adopted to validate the expression level of Tom1L1 in the two groups. Furthermore, 34 patients with locally progressive mid-low rectal adenocarcinoma, who were treated with neoadjuvant Xelox chemotherapy prior to the operation, IHC was adopted to detect the expression of Tom1L1 protein in patients before and after neoadjuvant chemotherapy and to analyze the relationship between the expression level of Tom1L1 and the sensitivity of neoadjuvant therapy.

resultsThe results of qPCR, Western blot and IHC showed that the expression of Tom1L1 in colorectal adenocarcinoma tissues was significantly higher than that in paracancerous normal tissues, with a statistically significant difference (P < 0.01); Neoadjuvant chemotherapy was significantly more effective in patients with low expression of Tom1L1 protein than in those with high expression of Tom1L1 protein, with a statistically significant difference (P < 0.05).

conclusionsTom1L1 is highly expressed in colorectal adenocarcinoma tissues; neoadjuvant Xelox chemotherapy can have an impact on Tom1L1 expression in progressive rectal cancer; patients with locally progressive mid-low rectal adenocarcinoma who have low Tom1L1 expression are more sensitive to neoadjuvant chemotherapy.

Indexed as

Adaptor Proteins, Signal TransducingAdenocarcinomaAntineoplastic Combined Chemotherapy ProtocolsColorectal NeoplasmsRectal NeoplasmsCapecitabineCase-Control StudiesChemotherapy, AdjuvantDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansImmunohistochemistryNeoadjuvant TherapyOxaloacetatesPrognosisRectumAdaptor Proteins, Signal TransducingCapecitabineOxaloacetatesTOM1L1 protein, humanBiomarkerMid-low rectal adenocarcinomaNeoadjuvant chemotherapyTarget of Myb1-Like1

Identifiers

PMID39548458
PMCPMC11568529

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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.