Skip to main content

Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study

Abstract

Background

As a transmembrane protein, C-type lectin-like receptor 2 (CLEC-2) is mainly expressed on platelets and released into plasma after platelet activation. Activated platelets participate in the regulation of innate immune cells. Patients with different microsatellite statuses have distinct immune profiles. This study aimed to investigate the association of plasma CLEC-2 levels with microsatellite status among colorectal cancer (CRC) patients.

Methods

A cross-sectional analysis of 430 CRC patients from Harbin Medical University Cancer Hospital was conducted. CLEC-2 levels were measured with fasting venous blood samples drawn from each participant before any treatment. The microsatellite status was evaluated with DNA obtained from fresh frozen tumor tissue samples. The other clinical data were collected and recorded based on the medical system records.

Results

CLEC-2 levels were significantly higher among patients with high microsatellite instability phenotype than the stable microsatellite group, adjusting for other confounding variables.

Conclusions

The increased CLEC-2 is associated with the high microsatellite instability subtype of CRC.

Peer Review reports

Introduction

Colorectal cancer (CRC) ranked third in incidence and second in mortality according to the global cancer statistics in 2020 [1]. Environmental and genetic factors (gene mutations, chromosomal abnormalities, and epigenetic changes) are involved in CRC development [2]. Microsatellite instability (MSI) is caused by the impaired DNA mismatch repair system, including high MSI (MSI-H) and low MSI (MSI-L). MSI CRC is characterized by a high density of tumor-infiltrating lymphocytes located in the proximal colon, and a better prognosis than microsatellite stabilization (MSS) tumors, accounting for 15% in CRC without a family history [3, 4]. Tumors can induce platelet activation, and activated platelets could promote tumor progression and metastasis [5]. Mean platelet volume (MPV) is considered an indicator of platelet activation and decreased MPV is a poor prognostic marker for many cancers [6,7,8]. MPV is significantly reduced in the MSI-H subtype of CRC [9, 10].

C-type lectin-like receptor 2 (CLEC-2) is a type II transmembrane protein. It is mainly expressed on activated platelets and megakaryocytes and released into plasma after platelet activation [11]. Podoplanin, the only established endogenous ligand for CLEC-2, is described on the surface of tumors or lymphatic endothelial cells and stimulates platelet activation through CLEC-2 binding to promote blood-borne tumor metastasis or the separation of blood/lymphatic vessels at the developmental stage [12]. However, few studies evaluated CLEC-2 levels in patients with CRC. This study aimed to determine the plasma levels of CLEC-2 in CRC patients and investigate the associations between CLEC-2 levels and MSI status.

Methods

Study population

CRC patients aged 18 years and over were invited to participate in this cross-sectional study in Harbin Medical University Cancer Hospital from January 2018 to December 2018. CRC was identified by histology. Patients were excluded with the following condition: (1) any history of radiotherapy, chemotherapy, or other anti-cancer therapy; (2) infection, hematological disorders, hypertension, and diabetes mellitus; (3) medical treatment with statins and acetylsalicylic acid; (4) insufficient clinical data. The trained research assistant collected data about age, gender, body mass index (BMI), smoking status, and drinking status of all eligible participants with a well-designed questionnaire.

The clinical data were collected and recorded based on the medical system records, including albumin, creatinine, white blood cells (WBC), hemoglobin, platelet count, tumor location, tumor size, histological type, histological grade, venous invasion, perineural invasion, T classification, lymph node metastasis, and distant metastasis. The TNM stage was classified according to the 8th edition of the American Joint Committee on Cancer staging system.

CLEC-2 measurements

A venous blood sample was drawn from each participant under fasting conditions at primary diagnosis before any treatment. The blood samples were collected by tubes containing sodium citrate and separated by centrifugation at 2500 rpm for 10 minutes, and the plasma was stored at − 80 °C until enzymatic analysis. CLEC-2 levels were measured in the hospital clinical laboratory, using commercially available sandwich ELISA kits (Xinle, Shanghai, China, respectively). Samples were measured as duplicates. The intra- and inter-assay variations were below 8 and 10%, respectively.

MSI analysis

The MSI was evaluated with DNA obtained from fresh frozen tumor tissue samples, using polymerase chain reaction with primers amplifying the microsatellite markers (BAT25, BAT26, NR-21, NR-24, and NR-27). MSI was defined as ≥3 unstable markers, while MSS was < 3 unstable markers. No sample has only two unstable markers.

Statistical analysis

The numbers and percentages were reported for presenting categorical variables. The mean ± standard deviation (SD) was used for reporting normal distribution continuous data, and the median (interquartile range) for non-normally distributed data. The Student’s t test was used when comparing variables with normal distribution in two groups, and the Mann-Whitney U test for skewed-distributed data. The χ2 test was used to evaluate the differences of categorical variables between groups. Binary logistic regression was used to assess the association between clinicopathological factors with MSI-H status. A receiver operating characteristic (ROC) curve was drawn to determine a threshold value of CLEC-2 for differentiating MSS from MSI-H using MedCalc version 15.0. SPSS Statistics version 25.0 (SPSS Inc., Chicago, IL, USA) was used for statistical analysis, and p <  0.05 represents statistical significance.

Results

A total of 430 eligible CRC patients were included in the final analysis, of which 14.88% were MSI-H patients. Baseline characteristics were compared between patients with MSI-H and MSS. CRC patients with MSI-H had higher BMI, WBC, CLEC-2 levels, younger age and lower hemoglobin levels than patients with MSS (Table 1). MSI-H status was significantly associated with tumor location, tumor size, lymphatic invasion, lymph node metastasis, clinical stage, and histological type (Table 2).

Table 1 Clinical and laboratory characteristics of colorectal cancer patients with high microsatellite instability and microsatellite stable status
Table 2 Clinicopathological features of of colorectal cancer patients according to microsatellite instability status

The median value of CLEC-2 was 138.3 (range, 62.0–272.6). The optimal cutoff value determined by ROC analysis for the CLEC-2 was 166.3 for the MSI-H (Fig. 1). The specificity and sensitivity were 51.6 and 86.9%, respectively (AUC = 0.734, 95% CI: 0.663–0.805, p <  0.001). CRC patients were divided into two groups according to the cutoff value. Of the 430 patients, 81 patients (18.8%) were detected with CLEC-2 of greater than 166.3 pg/mL, while there were 349 patients (81.2%) whose CLEC-2 levels were less than or equal to 166.3 pg/mL. Association between CLEC-2 and clinicopathologic variables was presented in Table 3. There were significant differences between CLEC-2 levels and MSI status.

Fig. 1
figure 1

The analysis of receiver-operating characteristic (ROC) curves. Legends: Receiver operating characteristic curve for prediction of high microsatellite instability based on c-type lectin-like receptor 2 (CLEC-2) by enzyme-linked immunosorbent assay

Table 3 Baseline characteristics of colorectal cancer patients according to c-type lectin-like receptor 2 levels

All CRC patients were classified into quartiles according to their CLEC-2 levels, including quartile 1 (Q1) ≤ 104.7 pg/mL, 104.7 pg/mL < quartile 2 (Q2) ≤ 142.7 pg/mL, 142.7 pg/mL < quartile 3 (Q3) ≤ 157.6 pg/mL, and quartile 4 (Q4) > 157.6 pg/mL (Fig. 2). The percentages of CRC patients with MSI-H in each group were 5.6, 8.2, 13.1 and 33.0%, respectively. The results showed that the percentage of patients with MSI-H increased according to CLEC-2 levels.

Fig. 2
figure 2

The association between microsatellite instability status and c-type lectin-like receptor 2 levels among colorectal cancer patiens. Legends: The percentage of patients with high microsatellite instability (MSI-H) rose as c-type lectin-like receptor 2 (CLEC-2) levels increased in each quartile among colorectal cancer (CRC) patients

Logistic regression analysis was performed to evaluate the clinicopathological factors associated with MSI-H status. Eleven variables, including age, BMI, WBC, hemoglobin, CLEC-2, tumor size, tumor location, lymphatic invasion, histological type, lymph node metastasis, and clinical stage, were entered into the original equation. The factors significantly associated with MSI-H in the regression analysis included age, BMI, WBC, CLEC-2, tumor size, tumor location, and histological type (Table 4). Notably, higher CLEC-2 levels were associated with MSI-H after adjusting for other confounding variables.

Table 4 Associations between clinical factors and microsatellite instability status

Discussion

The current finding showed that CLEC-2 levels were strongly associated with MSI-H CRC after adjusting the confounding confounders.

As one of the most common cancer, the global burden of CRC is expected to increase by 60% in 2030 [13]. CRC is characterized by the gradual accumulation of malignant transformation involving multiple genetic changes, which is conducive to the proliferation and growth of tumor cells [14]. MMR is an important mechanism used by cells to repair damaged DNA. MMR recognizes and repairs DNA base insertions, deletions, and mismatches, which are caused by DNA polymerase slippage during replication [15]. Compared with normal cells, the mutation rate of cancer cells with MMR is 100 to 1000 times that of normal cells. MSI-H tumors tend to be mucinous and poorly differentiated, with an expansive growth pattern, histological heterogeneity, and tumor-infiltrating lymphocytes [15].

The exact mechanisms of CLEC-2 in MSI-H CRCs are currently unclear. Both CLEC-2 and microsatellite status have been confirmed to be related to platelet activation status, which may be their underlying mechanism [10, 11]. CLEC-2 plays an important role in body development, tumor progression and immune response [16]. In malignant tumors, CLEC-2 and podoplanin work together to activate platelets to promote tumor metastasis and promote tumor-related thrombosis [12]. The difference of CLEC-2 in different CRC subtypes supports the crucial roles that platelets play in immune cells. Previous studies showed that the CD8 T effector gene signature was significantly upregulated in MSI-H tumors compared with MSI-L/MSS tumors [17]. The abundance of podoplanin is related to the immune evasion environment characterized by the infiltration of tumor macrophages and dysfunctional CD8+ T cells [18]. The growth and progression of tumors are also affected by the abundant tumor-associated macrophages in the tumor microenvironment [19]. MSI-H and MSI-L CRC have different tumor microenvironments. MSI-H tumor cells are characterized by their high mutation rate leading to the presentation of mutant peptides on their major histocompatibility complex class I molecules. These processes, in turn, are recognized by immune cells as foreign neoantigens, leading to a high density of cytotoxic CD8+ T cells infiltration and increased levels of IFN-γ secretion. Moreover, CD8 (+) cytotoxic T lymphocytes may increase platelet destruction in immune thrombocytopenia [20].

The tumor cells coated by aggregates of platelets are easy to evade the immune system and adhere to the vessel wall [5]. The activated platelets also secrete various bioactive factors that assist in extravasation to new metastatic sites [21]. Podoplanin has been reported to contribute to cancer pathogenesis by promoting tumor cell invasion and spreading [22]. The increased podoplanin expression was observed in patients with colorectal adenocarcinoma [23]. Clustering of podoplanin by platelet CLEC-2 regulates several molecular pathways involved in tumor cell migration and invasion [24]. Increased plasma CLEC-2 levels were observed in acute coronary syndrome, thrombotic microangiopathy, and acute ischemic stroke, indicating the critical role of CLEC-2 in thrombo-inflammation [25,26,27].

This study has some potential limitations: Firstly, our results were sourced from a single hospital. Secondly, further study is needed to explain our results mechanistically. Finally, this study only included Chinese participants, and the current finding should be validated in other populations.

Conclusions

Increased CLEC-2 is associated with the MSI-H subtype of CRC. Further mechanistic research was needed.

Availability of data and materials

The datasets generated and/or analysed during the current study are not publicly available due to privacy or ethical restrictions in our institute but are available from the corresponding author on reasonable request.

Abbreviations

CRC:

Colorectal cancer

BMI:

Body mass index

MVP:

Mean platelet volume

MSI:

Microsatellite instability

MSI-H:

High MSI

MSI-L:

Low MSI

MMR:

Mismatch repair

MSS:

Microsatellite stable

ROC:

Receiver operating characteristic

SD:

Standard deviation

WBC:

White blood cells

References

  1. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021;71(3):209–49.

    Article  Google Scholar 

  2. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.

    Article  Google Scholar 

  3. Boland CR, Thibodeau SN, Hamilton SR, Sidransky D, Eshleman JR, Burt RW, et al. A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res. 1998;58(22):5248–57.

    CAS  PubMed  Google Scholar 

  4. Motta R, Cabezas-Camarero S, Torres-Mattos C, Riquelme A, Calle A, Figueroa A, et al. Immunotherapy in microsatellite instability metastatic colorectal cancer: Current status and future perspectives. J Clin Transl Res. 2021;7(4):511–22.

    CAS  PubMed  PubMed Central  Google Scholar 

  5. Gaertner F, Massberg S. Patrolling the vascular borders: platelets in immunity to infection and cancer. Nat Rev Immunol. 2019;19(12):747–60.

    Article  CAS  Google Scholar 

  6. Wu YY, Zhang X, Qin YY, Qin JQ, Lin FQ. Mean platelet volume/platelet count ratio in colorectal cancer: a retrospective clinical study. BMC Cancer. 2019;19(1):314.

    Article  CAS  Google Scholar 

  7. Yin JB, Niu Y, Qian LY, Zhang X, Liu ZP, Wang RT. Mean platelet volume predicts survival in patients with hepatocellular carcinoma and type 2 diabetes. Diabetes Res Clin Pract. 2019;151:120–7.

    Article  Google Scholar 

  8. Bv P, Anwar AZ, Harsha R, Arakeri PR, Jonnada P. Role of Mean Platelet Volume in the Prognosis of Gallbladder Carcinoma: A Tertiary Centre Experience. Cureus. 2021;13(7):e16389.

    PubMed  PubMed Central  Google Scholar 

  9. Wang W, Wang G, Fu S, Zhang B, Liu Z, Wang R. Decreased mean platelet volume is associated with microsatellite instability in colorectal cancer: A propensity score-matched analysis. Cancer Biomark. 2021;31(4):351–9.

    Article  CAS  Google Scholar 

  10. Park Y, Schoene N, Harris W. Mean platelet volume as an indicator of platelet activation: methodological issues. Platelets. 2002;13(5–6):301–6.

    Article  CAS  Google Scholar 

  11. Kazama F, Nakamura J, Osada M, Inoue O, Oosawa M, Tamura S, et al. Measurement of soluble C-type lectin-like receptor 2 in human plasma. Platelets. 2015;26(8):711–9.

    Article  CAS  Google Scholar 

  12. Suzuki-Inoue K. Platelets and cancer-associated thrombosis: focusing on the platelet activation receptor CLEC-2 and podoplanin. Blood. 2019;134(22):1912–8.

    Article  Google Scholar 

  13. Arnold M, Sierra MS, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global patterns and trends in colorectal cancer incidence and mortality. Gut. 2017;66(4):683–91.

    Article  Google Scholar 

  14. Fearon ER. Molecular genetics of colorectal cancer. Annu Rev Pathol. 2011;6:479–507.

    Article  CAS  Google Scholar 

  15. Kreidieh M, Mukherji D, Temraz S, Shamseddine A. Expanding the Scope of Immunotherapy in Colorectal Cancer: Current Clinical Approaches and Future Directions. Biomed Res Int. 2020;2020:9037217.

    Article  Google Scholar 

  16. Brown GD, Willment JA, Whitehead L. C-type lectins in immunity and homeostasis. Nat Rev Immunol. 2018;18(6):374–89.

    Article  CAS  Google Scholar 

  17. Kikuchi T, Mimura K, Okayama H, Nakayama Y, Saito K, Yamada L, et al. A subset of patients with MSS/MSI-low-colorectal cancer showed increased CD8(+) TILs together with up-regulated IFN-gamma. Oncol Lett. 2019;18(6):5977–85.

    CAS  PubMed  PubMed Central  Google Scholar 

  18. Liu X, Cao Y, Lv K, Gu Y, Jin K, He X, et al. Tumor-infiltrating podoplanin(+) cells in gastric cancer: clinical outcomes and association with immune contexture. Oncoimmunology. 2020;9(1):1845038.

    Article  Google Scholar 

  19. Zhou Q, Wang Z, Zeng H, Zhang H, Liu Z, Huang Q, et al. Identification and validation of poor prognosis immunoevasive subtype of muscle-invasive bladder cancer with tumor-infiltrating podoplanin(+) cell abundance. Oncoimmunology. 2020;9(1):1747333.

    Article  Google Scholar 

  20. Qiu J, Liu X, Li X, Zhang X, Han P, Zhou H, et al. CD8(+) T cells induce platelet clearance in the liver via platelet desialylation in immune thrombocytopenia. Sci Rep. 2016;6:27445.

    Article  CAS  Google Scholar 

  21. Catani MV, Savini I, Tullio V, Gasperi V. The "Janus Face" of Platelets in Cancer. Int J Mol Sci. 2020;21(3):788.

    Article  CAS  Google Scholar 

  22. Suzuki-Inoue K. Roles of the CLEC-2-podoplanin interaction in tumor progression. Platelets. 2018;129:1–7.

  23. Kato Y, Fujita N, Kunita A, Sato S, Kaneko M, Osawa M, et al. Molecular identification of Aggrus/T1alpha as a platelet aggregation-inducing factor expressed in colorectal tumors. J Biol Chem. 2003;278(51):51599–605.

    Article  CAS  Google Scholar 

  24. Lowe KL, Navarro-Nunez L, Watson SP. Platelet CLEC-2 and podoplanin in cancer metastasis. Thromb Res. 2012;129(Suppl 1):S30–7.

    Article  CAS  Google Scholar 

  25. Inoue O, Osada M, Nakamura J, Kazama F, Shirai T, Tsukiji N, et al. Soluble CLEC-2 is generated independently of ADAM10 and is increased in plasma in acute coronary syndrome: comparison with soluble GPVI. Int J Hematol. 2019;110(3):285–94.

    Article  Google Scholar 

  26. Yamashita Y, Suzuki K, Mastumoto T, Ikejiri M, Ohishi K, Katayama N, et al. Elevated plasma levels of soluble C-type lectin-like receptor 2 (CLEC2) in patients with thrombotic microangiopathy. Thromb Res. 2019;178:54–8.

    Article  CAS  Google Scholar 

  27. Zhang X, Zhang W, Wu X, Li H, Zhang C, Huang Z, et al. Prognostic Significance of Plasma CLEC-2 (C-Type Lectin-Like Receptor 2) in Patients With Acute Ischemic Stroke. Stroke. 2018;50:STROKEAHA118022563.

Download references

Acknowledgments

Not applicable.

Funding

This study was supported by the Haiyan Foundation of Harbin Medical University Cancer Hospital (JJQN2019–06).

Author information

Authors and Affiliations

Authors

Contributions

Xin Zhang and Jia-rui Yuan proposed and designed the study; Xin Wang and Shuang Fu collected data; Rui-tao Wang and Guang-yu Wang analyzed the data, interpreted the results, and drafted the article. Every author approved the final version of the manuscript for publishing.

Corresponding authors

Correspondence to Rui-tao Wang or Guang-yu Wang.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the Institutional Review Board of Harbin Medical University Cancer Hospital (2017-C-352) and performed according to the declaration of Helsinki. All patients voluntarily participated in this study with written informed consent.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zhang, X., Yuan, Jr., Wang, X. et al. Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study. BMC Cancer 22, 823 (2022). https://doi.org/10.1186/s12885-022-09834-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12885-022-09834-4

Keywords